Prodrugs of dithiol mucolytic agents

ABSTRACT

Provided are mucolytic compounds that are more effective, and/or absorbed less rapidly from mucosal surfaces, and/or are better tolerated as compared to N-acetylcysteine (NAC) and DTT. The compounds are represented by compounds of Formula I which embrace structures (Ia)-(Ib): 
                         
where the structural variables are as defined herein.

CONTINUING APPLICATION INFORMATION

The present application claims benefit of U.S. provisional application Ser. No. 62/155,078, filed on Apr. 30, 2015, and incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

Field of the Invention

The present invention is directed to mucolytic compounds that are more effective, and/or absorbed less rapidly from mucosal surfaces, and/or are better tolerated as compared to N-acetylcysteine (NAC) and DTT.

Description of the Background

Many modern drugs are discovered through high-throughput screening or combinatorial chemistry. These compounds often are selected for their high pharmacological efficacy but unintentionally have poor drug-like characteristics (e.g., solubility, bioavailability, stability). One strategy to overcome these physiochemical, biopharmaceutical, and pharmacokinetic limitations is to use a prodrug form of the compound, a molecule that is inactive until undergoing an enzymatic or chemical transformation in vivo. Depending on the type of modification, prodrugs can have key advantages over their active counterparts: 1) low/no odor until activated, 2) increased stability and shelf-life, 3) increased aqueous solubility, 4) improved bioavailability, 5) improved oral absorption, 6) increased lipophilicity/permeability, and 7) improved parenteral administration.

Of the drugs approved worldwide, 5-7% can be classified as prodrugs. These drugs are classified into two categories, bioprecurser prodrugs or carrier-linked prodrugs. Bioprecurser prodrugs are converted into pharmacologically active drugs by metabolic or chemical transformation. Carrier-linked prodrugs have a promoiety that is covalently linked to an active parent molecule. This promoiety is released, usually by enzymatic hydrolysis, activating the parent molecule once delivered to the therapeutic location. Design of the prodrug moiety is usually based on the drug-like characteristics that need improvement in a particular molecule, the available functional groups that are amenable to a promoiety, and the targeted organ or tissue. In cases where the promoiety cannot be directly attached due to reasons such as steric hinderance, spacers or linkers are also added. In order to be well-tolerated, the promoiety should be non-immunogenic, stable until reaching the therapeutic tissue, and rapidly excreted from the body, once cleaved from the parent. Esters are one of the most commonly used promoieties, due to their ease of removal from the parent drug by ubiquitous esterases (e.g., acetylcholinesterases, butyrylcholinesterases, carboxylesterases, arlesterases), capability of increasing drug solubility by masking charge groups, such as carboxylic acids and phophates, and relatively simple synthesis. Some other common functional groups that are utilized as promoieties are: carbonates, carbamates, amides, phosphates, and oximes.

Prodrugs could be particularly useful as inhaled therapeutics for muco-obstructive respiratory diseases, such as chronic bronchitis (CB), including the most common lethal genetic form of chronic bronchitis, cystic fibrosis (CF). In a normally functioning lung, the primary defense against chronic intrapulmonary airways infection (chronic bronchitis) is mediated by the continuous clearance of mucus from bronchial airway surfaces, removing potentially noxious toxins and pathogens from the lung. In a healthy lung, the airway surface liquid is primarily composed of salt and water in proportions similar to plasma (i.e., isotonic). Ion transport properties regulate the amount of salt and water, and goblet cells and glands control the quantity of mucins on the airway surface. Mucin macromolecules organize into a well-defined mucus layer, which traps inhaled bacteria and is transported out of the lung via the actions of cilia, which beat in a watery, low viscosity solution termed the periciliary liquid. When there is an imbalance of the mucin to liquid ratio, the mucus becomes excessively viscous and adherent, which can lead to airway mucus accumulation and infection because the cilia cannot beat to clear the mucus.

Recent data indicate that the basic defect in both CB and CF is the failure to clear mucus from airway surfaces. As described above, the failure to clear mucus reflects an imbalance between the amount of airway surface liquid and mucin on airway surfaces. Patients with mucus-obstructive diseases, including CF, CB associated with cigarette smoke exposure (i.e., COPD), and asthma, exhibit increases in mucus concentration, as quantified by % solids (FIG. 1), as a result of reduced airway hydration and mucin hypersecretion due to goblet cell and glandular hyperplasia. Both as a function of disease severity, and in acute exacerbations, raised mucin concentrations produce adherent mucus that sticks to epithelial cells, impairs clearance, and triggers inflammatory responses and airway wall injury. The reduction in mechanical clearance of mucus from the lung leads to chronic bacterial colonization of mucus adherent to airway surfaces. It is the chronic retention of bacteria, the failure of local antimicrobial substances to kill mucus-entrapped bacteria on a chronic basis, and the subsequent chronic inflammatory responses of the body to this type of surface infection, that lead to the syndromes of CB and CF. Therefore, enhancing the clearance of such thickened, adhered mucus from the airways is likely to benefit patients with these mucus-obstructive diseases.

The current afflicted population in the U.S. is 12,000,000 patients with the acquired (primarily from cigarette smoke exposure) form of chronic bronchitis and approximately 30,000 patients with the genetic form, cystic fibrosis. Approximately equal numbers of both populations are present in Europe. In Asia, there is little CF but the incidence of CB is high and, like the rest of the world, is increasing.

There is currently a large, unmet medical need for products that specifically treat CB and CF at the level of the basic defect that cause these diseases. The current therapies for chronic bronchitis and cystic fibrosis focus on treating the symptoms and/or the late effects of these diseases. Thus, for chronic bronchitis, 3-agonists, inhaled steroids, anti-cholinergic agents, and oral theophyllines and phosphodiesterase inhibitors are all in development. However, none of these drugs effectively treat the fundamental problem of the failure to clear mucus from the lung. Similarly, in cystic fibrosis, the same spectrum of pharmacologic agents is used. These strategies have been complemented by more recent strategies designed to clear the CF lung of the DNA (“Pulmozyme®”; Genentech) that has been deposited in the lung by neutrophils that have futilely attempted to kill the bacteria that grow in adherent mucus masses and through the use of inhaled antibiotics (“TOBI®”) designed to augment the lungs' own killing mechanisms to rid the adherent mucus plaques of bacteria. A general principle of the body is that if the initiating lesion is not treated, in this case mucus retention/obstruction, bacterial infections become chronic and increasingly refractory to antimicrobial therapy. Thus, a major unmet therapeutic need for both CB and CF lung diseases is an effective means of mobilizing airway mucus and promoting its clearance, with bacteria, from the lung.

In addition to CB and CF lung diseases, there is a large unmet need to facilitate the clearance of excess mucus secretions from the lungs in other mucoobstructive conditions. The overproduction of pulmonary mucus has been characterized in conditions including idiopathic pulmonary fibrosis, asthma, viral and bacterial lung infections, primary ciliary dyskinesia, and non-CF bronchiectasis, and mechanical lung ventilation. The accumulation of pulmonary mucus can harbor bacteria leading to chronic lung infections, as well as, reduces lung function. Thus, there is a need for therapeutic agents which facilitate the clearance of excess mucus.

Other mucosal surfaces in and on the body exhibit subtle differences in the normal physiology of the protective surface liquids on their surfaces, but the pathophysiology of disease reflects a common theme: an imbalance in the composition of the protective surface liquid and impaired mucus clearance. For example, in xerostomia (dry mouth) the oral cavity is depleted of liquid due to a failure of the parotid sublingual and submandibular glands to secrete liquid.

Similarly, keratoconjunctivitis sicca (dry eye) is caused insufficient tear volume resulting from the failure of lacrimal glands to secrete liquid or excessive evaporative fluid loss. In rhinosinusitis, there is an imbalance, as in CB, between mucin secretion, relative airway surface liquid depletion, and mucus stasis. Finally, in the gastrointestinal tract, failure to secrete Cl⁻ (and liquid) in the proximal small intestine combined with increased Na⁺ (and liquid) absorption in the terminal ileum leads to the distal intestinal obstruction syndrome (DIOS). In older patients, excessive Na⁺ (and volume) absorption in the descending colon produces constipation and diverticulitis.

The high prevalence of both acute and chronic bronchitis indicates that this disease syndrome is a major health problem in the U.S. Despite significant advancements in the etiology of mucus obstructive diseases, pharmacotherapy of both CF and COPD have been characterized by an aging array of therapies, typically including inhaled steroids and bronchodilators for maintenance, and antibiotics and high-dose steroids for exacerbations. Clearly, drugs are needed that are more effective at restoring the clearance of mucus from the lungs of patients with CB/CF. The value of these new therapies will be reflected in improvements in the quality and duration of life for both the CF and the CB populations.

One approach to increase mucus clearance is to enhance the transportability of mucins via the disruption of the polymeric mucus structure. Mucin proteins are organized into high molecular weight polymers via the formation of covalent (disulfide) and non-covalent bonds. Disruption of the covalent bonds with reducing agents is a well-established method to reduce the viscoelastic properties of mucus in vitro and is predicted to minimize mucus adhesiveness and improve clearance in vivo. Reducing agents are well known to decrease mucus viscosity in vitro and commonly used as an aid to processing sputum samples (Hirsch, S. R., Zastrow, J. E., and Kory, R. C. Sputum liquefying agents: a comparative in vitro evaluation. J. Lab. Clin. Med. 1969. 74:346-353). Examples of reducing agents include sulfide containing molecules capable of reducing protein disulfide bonds including, but not limited to, N-acetyl cysteine, N-acystelyn, carbocysteine, cysteamine, glutathione, and thioredoxin containing proteins.

N-acetyl cysteine (NAC) is approved for use in conjunction with chest physiotherapy to loosen viscid or thickened airway mucus. Clinical studies evaluating the effects of oral or inhaled NAC in CF and COPD have reported improvements in the rheologic properties of mucus and trends toward improvements in lung function and decreases in pulmonary exacerbations (Duijvestijn Y C M and Brand P L P. Systematic review of N-acetylcysteine in cystic fibrosis. Acta Peadiatr 88: 38-41. 1999). However, the preponderance of clinical data suggests that NAC is at best a marginally effective therapeutic agent for treating airway mucus obstruction when administered orally or as an inhalation aerosol. A recent Cochrane review of the existing clinical literature on the use of NAC found no evidence to support the efficacy of NAC for CF (Tam J, Nash E F, Ratjien F, Tullis E, Stephenson A; Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis. Cochrane Database Syst Rev. 2013; 12(7):CD007168.).

NAC, as a topical pulmonary therapeutic agent, is not optimal for the reduction of mucin disulfide bonds. Specifically, NAC does not possess the basic properties of an effective pulmonary drug as NAC (1) is a relatively inefficient reducing agent the airway surface environment (e.g., CF pH 6.5-7.2); and (2) is rapidly metabolized and cleared from the airway surface (Jayaraman S, Song Y, Vetrivel L, Shankar L, Verkman A S. Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH. J Clin Invest. 2001; 107(3):317-24). For example, in the pH environment of the airway surface (measured in the range of pH 6.0 to 7.2 in CF and COPD airways), NAC exists only partially in its reactive state as a negatively charge thiolate (Jayaraman S, Song Y, Vetrivel L, Shankar L, Verkman A S. Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH. J Clin Invest. 2001; 107(3):317-24). Furthermore, in animal studies, ¹⁴C-labeled NAC, administered by inhalation, exhibits rapid elimination from the lungs with a half-life of approximately 20 minutes (unpublished observation). The relatively low reducing activity at of NAC physiologic airway pH and the short half-life of NAC on the lung surface provide an explanation for the lack of strong clinical evidence for effective mucus reduction in mucus obstructive diseases.

Additionally, NAC is most commonly administered as a concentrated inhalation solution (Mucomysrt is a 20% or 1.27M solution). However, the administration of concentrated NAC solutions impact the tolerability of NAC as it exaggerates (1) the unpleasant sulfur taste/odor; and (2) pulmonary side effects including irritation and bronchoconstriction which can require co-administration of rescue medications such as bronchodilators. Although Mucomysta was approved by the FDA in 1963, no other reducing agents administered as an inhalation aerosol are currently available to treat muco-obstructive diseases. What are needed are effective, safe, and well-tolerated reducing agents for the treatment of diseases characterized by impaired mucus clearance.

As discussed above, compounds that could be useful in the treatment of muco-obstructive diseases as mucolytics often contain sulfides. These drugs, like NAC and DTT, typically have an unpleasant sulfurous odor/taste, can be oxidized (i.e., inactivated) easily, and are less tolerated. The addition of prodrug moieties could be a useful strategy to overcome these limitations to produce novel, well-tolerated therapeutics for a number of muco-obstructive diseases.

SUMMARY OF THE INVENTION

One object of the present invention relates to a method to increase the liquefaction of mucus in a patient with excessive mucus or mucus with increased viscoelastic, cohesive, or adhesive properties. The method includes the step of contacting the mucus of a patient with abnormal or excessive mucus with a composition comprising a mucolytic compound containing a dithiol group to decrease mucus viscoelasticity through the reduction of mucin disulfide bonds.

It is an object of the present invention to provide mucolytic compounds that are more effective, and/or absorbed less rapidly from mucosal surfaces, and/or are better tolerated as compared to N-acetylcysteine (NAC) and DTT.

It is another object of the present invention to provide compounds which are more active in the physiologic environment of the airway surface.

It is another object of the present invention to provide compounds that are more potent and/or absorbed less rapidly, as compared to compounds such as N-acetylcysteine and DTT.

Therefore, such compounds will give a prolonged pharmacodynamic half-life on mucosal surfaces as compared to NAC and DTT.

It is another object of the present invention to provide methods of treatment that take advantage of the pharmacological properties of the compounds described above.

In particular, it is an object of the present invention to provide methods of treatment which rely on promoting mucus clearance from mucosal surfaces.

It is an object of the present invention to provide compounds that are more potent and/or absorbed less rapidly from mucosal surfaces, and/or are less reversible as compared to known compounds.

Therefore, the compounds will give a prolonged pharmacodynamic half-life on mucosal surfaces as compared to known compounds.

It is another object of the present invention to provide compounds which are (1) absorbed less rapidly from mucosal surfaces, especially airway surfaces, as compared to known compounds and; (2) It is another object of the present invention to provide compounds that are more potent and/or absorbed less rapidly and/or exhibit less reversibility, as compared to compounds such as DTT and NAC. Therefore, such compounds will give a prolonged pharmacodynamic half-life on mucosal surfaces as compared to previous compounds.

It is another object of the present invention to provide methods of treatment that take advantage of the pharmacological properties of the compounds described above.

In particular, it is an object of the present invention to provide methods of treatment which rely on rehydration of mucosal surfaces.

The objects of the present invention may be accomplished with a class of dithiols represented by compounds of Formula I which embraces structures (Ia)-(Ib):

wherein

R¹ and R² are each, independently, hydrogen, lower alkyl, halogen or triflouromethyl;

R³ and R⁴ are each, independently, hydrogen, lower alkyl, hydroxyl-lower alkyl, phenyl, (phenyl)-lower alkyl, (halophenyl)-lower alkyl, ((lower-alkyl)phenyl)-lower-alkyl, ((lower-alkoxy)phenyl)-lower-alkyl, (naphthyl)-lower-alkyl, or (pyridyl)-lower-alkyl;

each R⁵ is, independently, hydrogen, halogen, trifluoromethyl, lower alkyl, unsubstituted or substituted phenyl, lower alkyl-thio, phenyl-lower alkyl-thio, lower alkyl-sulfonyl, or phenyl-lower alkyl-sulfonyl, OH, —(CH₂)_(m)—OR⁸, —O—(CH₂)_(m)—OR⁸, —(CH₂)—NR⁷R¹⁰, —(CH₂)—NR⁷R⁷, —O—(CH₂)_(m)—NR⁷R¹⁰, —O—(CH₂)_(m)—NR⁷R⁷, —(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)(CHOR⁸)(CHOR⁸)—CH₂OR⁸, —(CH₂CH₂O)_(m)—R⁸, —O—(CH₂CH₂O)_(m)—R⁸, —(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —O—(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —(CH₂)_(n)—C(═O)NR⁷R¹⁰, —O—(CH₂)_(m)—C(═O)NR⁷R¹⁰, —(CH₂)_(n)—(Z)_(g)—R⁷, —O—(CH₂)_(m)—(Z)_(g)—R⁷, —(CH₂)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)—CH₂OR⁸, —(CH₂)_(n)—CO₂R⁷, —O—(CH₂)_(m)—CO₂R⁷, —OSO₃H, —O-glucuronide, —O-glucose,

-Link-(CH₂)_(m)-CAP, -Link-(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂CH₂O)_(m)—CH₂-CAP, -Link-(CH₂CH₂O)_(m)—CH₂CH₂-CAP, -Link-(CH₂)_(m)—(Z)_(g)-CAP, -Link-(CH₂)_(n)(Z)_(g)—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—NR¹³—CH₂(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂)_(n)—(CHOR⁸)_(m)CH₂—NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(n)NR¹³—(CH₂)_(m)(CHOR⁸)_(n)CH₂NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(m)—(Z)_(g)—(CH₂)_(m)-CAP, -Link-NH—C(═O)—NH—(CH₂)_(m)-CAP, -Link-(CH₂)_(m)—C(═O)NR¹³—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—(Z)_(g)—(CH₂)_(m)—(Z)_(g)-CAP, or -Link-Z_(g)—(CH₂)_(m)-Het-(CH₂)_(m)-CAP with the proviso that at least one R⁵ group contains at least one basic nitrogen;

each R⁷ is, independently, hydrogen, lower alkyl, phenyl, substituted phenyl, lower alkyl phenyl or —CH₂(CHOR⁸)_(m)—CH₂OR⁸;

each R⁸ is, independently, hydrogen, lower alkyl, lower alkyl phenyl, —C(═O)—R¹¹, glucuronide,

2-tetrahydropyranyl, or

each R⁹ is, independently, —CO₂R⁷, —CON(R⁷)₂, —SO₂CH₃, —C(═O)R⁷, —CO₂R¹³, —CON(R¹³)₂, —SO₂CH₂R¹³, or —C(═O)R¹³;

each R¹⁰ is, independently, —H, —SO₂CH₃, —CO₂R⁷, —C(═O)NR⁷R⁹, —C(═O)R⁷, or —CH₂—(CHOH)_(n)—CH₂OH;

each Z is, independently, —(CHOH)—, —C(═O)—, —(CHNR⁷R¹⁰)—, —(C═NR¹⁰)—, —NR¹⁰—, —(CH₂)_(n)—, —(CHNR¹³R¹³)—, —(C═NR¹³)—, or —NR¹³—;

each R¹¹ is, independently, hydrogen, lower alkyl, phenyl lower alkyl or substituted phenyl lower alkyl;

each R¹² is, independently, —SO₂CH₃, —CO₂R⁷, —C(═O)NR⁷R⁹, —C(═O)R⁷, —CH₂(CHOH)_(n)—CH₂OH, —CO₂R¹³, —C(═O)NR¹³R¹³, or —C(═O)R¹³;

each R¹³ is, independently, hydrogen, lower alkyl, phenyl, substituted phenyl or —CH₂(CHOR⁸)_(m)—CH₂OR⁸, —SO₂CH₃, —CO₂R⁷, —C(═O)NR⁷R⁹, —C(═O)R⁷, —CH₂—(CHOH)_(n)—CH₂OH, —(CH₂)_(m)—NR⁷R¹⁰, —(CH₂)_(m)—NR⁷R⁷, (CH₂)_(m)—NR¹¹R¹¹, —(CH₂)_(m)—(NR¹¹R¹¹R¹¹)⁺, (CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)NR¹¹R¹¹, —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)NR⁷R¹⁰, —(CH₂)_(m)—NR¹⁰R¹⁰, —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)—(NR¹¹R¹¹R¹¹)⁺, —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)NR⁷R⁷;

each R¹⁴ is, independently, hydrogen, —C(═O)—R⁷, or an Amino Acyl of the natural configuration with the proviso that at least one R¹⁴ is other than H;

each g is, independently, an integer from 1 to 6;

each m is, independently, an integer from 1 to 7;

each n is, independently, an integer from 0 to 7;

each -Het- is, independently, —N(R⁷)—, —N(R¹⁰)—, —S—, —SO—, —SO₂—; —O—, —SO₂NH—, —NHSO₂—, —NR⁷CO—, —CONR⁷—, —N(R¹³)—, —SO₂NR¹³—, —NR¹³CO—, or —CONR¹³—;

each Link is, independently, —O—, —(CH₂)_(n)—, —O(CH₂)_(m)—, —NR¹³—C(═O)—NR¹³—, —NR¹³—C(═O)—(CH₂)_(m), —C(═O)NR¹³—(CH₂)_(m)—, —(CH₂)_(n)—(Z)_(g)—(CH₂)_(n)—, —S—, —SO—, —SO₂—, —SO₂NR⁷—, —SO₂NR¹¹—, or -Het-;

each CAP is, independently

with the proviso that when any —CHOR⁸— or —CH₂OR⁸ groups are located 1,2- or 1,3- with respect to each other, the R⁸ groups may, optionally, be taken together to form a cyclic mono- or di-substituted 1,3-dioxane or 1,3-dioxolane;

and racemates, enantiomers, diastereomers, tautomers, polymorphs, pseudopolymorphs and pharmaceutically acceptable salts, thereof.

The present invention also provides pharmaceutical compositions which comprise a compound as described herein.

The present invention also provides a method of restoring mucosal defense, comprising: contacting mucus with an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of decreasing mucus viscoelasticity, comprising:

administering an effective amount of a compound described herein to a mucosal surface of a subject.

The present invention also provides a method of decreasing mucus viscoelasticity on a mucosal surface, comprising:

administering an effective amount of a compound described herein to a mucosal surface of a subject.

The present invention also provides a method of scavenging free radicals on a mucosal surface, comprising:

administering an effective amount of a compound described herein to a mucosal surface of a subject.

The present invention also provides a method of decreasing inflammation on a mucosal surface, comprising:

administering an effective amount of a compound described herein to a mucosal surface of a subject.

The present invention also provides a method of reducing inflammatory cells on a mucosal surface, comprising:

administering an effective amount of a compound described herein to a mucosal surface of a subject.

The present invention also provides a method treating mucus obstructive diseases, comprising:

contacting mucus with an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method treating mucus adhesion, comprising:

contacting mucus with an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of treating chronic bronchitis, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating cystic fibrosis, comprising:

administering an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of treating cystic fibrosis exacerbations, comprising:

administering an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of treating bronchiectasis, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating chronic obstructive pulmonary disease, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating chronic obstructive pulmonary disease exacerbations, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating asthma, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating asthma exacerbations, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating esophagitis, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating ventilator-induced pneumonia, comprising:

administering an effective compound described herein to a subject by means of a ventilator.

The present invention also provides a method of treating primary ciliary dyskinesia, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating emphysema, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating pneumonia, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating rhinosinusitis, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating nasal dehydration, comprising:

administering an effective amount of a compound described herein to the nasal passages of a subject in need thereof.

In a specific embodiment, the nasal dehydration is brought on by administering dry oxygen to the subject.

The present invention also provides a method of treating sinusitis, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating dry eye, comprising:

administering an effective amount of a compound described herein to the eye of the subject in need thereof.

The present invention also provides a method of promoting ocular hydration, comprising:

administering an effective amount of a compound described herein to the eye of the subject.

The present invention also provides a method of promoting corneal hydration, comprising:

administering an effective amount of a compound described herein to the eye of the subject.

The present invention also provides a method of treating excessive eye discharge produced by, but not limited to blepharitis, allergies, conjunctivitis, corneal ulcer, trachoma, congenital herpes simplex, corneal abrasions, ectropion, eyelid disorders, gonococcal conjunctivitis, herpetic keratitis, ophthalmitis, Sjogren's Syndrome, Stevens-Johnson Syndrome comprising:

administering an effective amount of a compound described herein to the eye of the subject.

The present invention also provides a method of treating Sjögren's disease, comprising:

administering an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of treating dry mouth (xerostomia), comprising:

administering an effective amount of compound described herein to the mouth of the subject in need thereof.

The present invention also provides a method of treating vaginal dryness, comprising:

administering an effective amount of a compound described herein to the vaginal tract of a subject in need thereof.

The present invention also provides a method of treating constipation, comprising:

administering an effective amount of a compound described herein to a subject in need thereof. In one embodiment of this method, the compound is administered either orally or via a suppository or enema.

The present invention also provides a method of treating distal intestinal obstruction syndrome, comprising:

administering an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of treating chronic diverticulitis comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of inducing sputum for diagnostic purposes, comprising:

administering an effective amount of compound described herein to a subject in need thereof.

The present invention also provides a method of treating inhaled pathogens, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating inhaled irritants, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

The present invention also provides a method of treating inhaled particles, comprising:

administering an effective amount of a compound described herein to a subject in need thereof.

In a specific embodiment, the inhaled particles are insoluble particles including dust, debris, or radioactive material.

The objects of the invention may also be accomplished with a method of treating anthrax, comprising administering an effective amount of a compound of Formula I as defined herein and an osmolyte to a subject in need thereof.

The objects of the invention may also be accomplished with a method of prophylactic, post-exposure prophylactic, preventive or therapeutic treatment against diseases or conditions caused by pathogens, particularly pathogens which may be used in bioterrorism, comprising administering an effective amount of a compound of Formula I to a subject in need thereof.

It is further an object of the present invention to provide treatments comprising the use of osmolytes together with mucolytics of Formula I that are more potent, more specific, and/or absorbed less rapidly from mucosal surfaces as compared to compounds such as NAC.

It is another aspect of the present invention to provide treatments using mucolytics of Formula I that are more potent and/or absorbed less rapidly and/or exhibit less reversibility, as compared to compounds such as NAC when administered with an osmotic enhancer. Therefore, such mucolytics when used in conjunction with osmolytes will give an increased pharmacodynamic effect on mucosal surfaces as compared to either compound used alone.

It is another object of the present invention to provide treatments using mucolytics of Formula I and osmolytes together which are absorbed less rapidly from mucosal surfaces, especially airway surfaces than NAC. It is another object of the invention to provide compositions which contain mucolytics of Formula I and osmolytes.

The objects of the invention may be accomplished with a method of treating a disease ameliorated by increased mucus clearance and mucosal hydration comprising administering an effective amount of a compound of Formula I as defined herein and an osmolyte to a subject in need of increased mucociliary clearance and/or mucosal hydration.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Role of mucus dehydration in pathogenic sequence of CF/COPD. (A) Normal conditions. (B) Disease-related dehydration of mucus (↑% solids), leads to a collapse of the periciliary layer (PCL), reduction or cessation of mucus clearance, and adhesion of the mucus layer to the cell surface.

FIG. 2. Capped dithiol compounds tested by DTNB before and after addition of aminopeptidase. The activity of compound 35, which has a peptide cap, and its parent compound, compound 41, was compared in a DTNB assay. Compound 35 was tested alone and after incubation with two concentrations of human aminopeptidase. Even after over an hour incubation with aminopeptidase, the enzyme does not completely activate the compound in this assay.

FIG. 3. Capped dithiol compounds tested by DTNB before and after addition of esterase. The acetate prodrug compound 11 and its base case, compound 41, were compared in a DTNB assay (top). Incubation with a low and high concentration of esterase for approximately 15 min. activated compound 11 to a similar level as compound 41, whereas compound 11 incubated for the same amount of time without esterase remained inactive. Compound 41 was also compared to the acetate prodrug compound 13 in a DTNB assay (bottom). The compound was fully activated immediately with the high concentration of esterase and near fully activated after a 15 min incubation with the low concentration.

FIG. 4. A capped dithiol compound tested by DTNB before and after addition of increasing amounts of esterase. The acetate prodrug compound 23 was incubated with varying amounts of esterase enzyme and tested for reducing activity via DTNB assay. Increasing amounts of esterase increased activation. The parent, compound 43 was fully activated in the same assay without enzyme.

FIG. 5. Stability comparison of capped and uncapped Parion compounds tested with DTNB. Parent drug, compound 43, was tested for stability by testing with DTNB after 4 days at room temperature (left). Acetate-capped compound, compound 23, was tested before and after incubation with esterase (right). The acetate cap prevents some but not all oxidation after 4 days.

FIG. 6. A capped dithiol compound tested by DTNB. Parion compound, compound 13, was tested for activation in a DTNB assay after incubation with varying amounts of esterase. Increasing amounts of esterase correlated with increasing activation. In this assay, compound 13 was fully activated when incubated with 0.015 units or higher.

FIG. 7. Western blot analysis of HBE mucus treated with compound 43 or compound 23. Reduction of mucus from the apical surface of HBE cultures was detected via western blot after a single treatment with vehicle (PBS), 10 mM parent drug (compound 43), or 10 mM prodrug (compound 23). Although slower than the compound 43, compound 23 reduced Muc5AC (left) and Muc5B (right) on the apical surface of HBE cultures. Time of incubation is indicated in hours.

FIG. 8. Western blot analysis of HBE mucus treated with compound 43 or compound 23. Reduction of mucus from the apical surface of HBE cultures was detected via western blot after a single treatment with vehicle (PBS), 10 mM parent drug (compound 43), or 10 mM prodrug (compound 23). Although slower than the compound 43, compound 23 reduced Muc5AC (left) and Muc5B (right) on the apical surface of HBE cultures. Time of incubation is indicated in hours.

FIG. 9. Membrane permeability assessed by PAMPA for various compounds. The data demonstrate that the compounds tested do not preferentially traverse a lipid bilayer, a property which is predicted to extend pulmonary surface retention.

FIG. 10. Mucin reduction (Muc5B) in cystic fibrosis sputum in vitro. All compounds were incubated with sputum at a final concentration of 10 mM for the indicated time (in hours) and assayed by agarose gel electrophoresis/western blot.

FIG. 11. Mucin reduction (Muc5B) in cystic fibrosis sputum in vitro. All compounds were incubated with sputum at a final concentration of 10 mM for the indicated time (in hours) and assayed by agarose gel electrophoresis/western blot.

FIG. 12. Mucin reduction (MucSB) in cystic fibrosis sputum in vitro with Compound 68. The compound was incubated with sputum at the indicated final concentration for 2 or 4 hours and assayed by agarose gel electrophoresis/western blot.

FIG. 13. Integrated metabolism and oxidation of Compound 68 on the apical surface of HBE cultures. At four hours post-dose, compound 68 was substantially metabolized and oxidized (indicating reaction with disulfide target). Furthermore, Compound 68 is substantially maintained on the apical cell surface, consistent with resistance to cellular permeation.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, the following terms are defined as indicated.

“A compound of the invention” means a compound of Formula I or a salt, particularly a pharmaceutically acceptable salt thereof.

“A compound of Formula I” means a compound having the structural formula designated herein as Formula I, which embraces structures (Ia) and (Ib). Compounds of Formula I include solvates and hydrates (i.e., adducts of a compound of Formula I with a solvent). In those embodiments wherein a compound of Formula I includes one or more chiral centers, the phrase is intended to encompass each individual stereoisomer including optical isomers (enantiomers and diastereomers) and geometric isomers (cis-/trans-isomerism) and mixtures of stereoisomers. In addition, compounds of Formula I also include tautomers of the depicted formula(s).

Throughout the description and examples, compounds are named using standard IUPAC naming principles, where possible, including the use of the ChemDraw Ultra 11.0 software program for naming compounds, sold by CambridgeSoft Corp./PerkinElmer.

In some chemical structure representations where carbon atoms do not have a sufficient number of attached variables depicted to produce a valence of four, the remaining carbon substituents needed to provide a valence of four should be assumed to be hydrogen. Similarly, in some chemical structures where a bond is drawn without specifying the terminal group, such bond is indicative of a methyl (Me, —CH₃) group, as is conventional in the art.

The present invention is based on the discovery that the compounds of Formula I are more potent and/or, absorbed less rapidly, achieve higher concentrations and have higher residence time in the mucosal surfaces, especially airway surfaces, and/or are better tolerated compared to NAC and DT. Therefore, the compounds of Formula I have a greater activity and/or produce less cellular toxicity on mucosal surfaces as compared to NAC and DTT.

The present invention is based on the discovery that the compounds of formula (I) are more potent and/or, absorbed less rapidly from mucosal surfaces, especially airway surfaces, and/or less reversible from interactions as compared to compounds such as NAC and DTT.

Therefore, the compounds of formula (I) have a longer half-life on mucosal surfaces as compared to these compounds.

In the compounds represented by formula I which embraces structures (Ia)-(Ib):

R¹ is hydrogen, lower alkylkoxy, halogen or triflouromethyl;

R² is hydrogen, lower alkyl, halogen or triflouromethyl;

R³ and R⁴ are each, independently, hydrogen, lower alkyl, hydroxyl-lower alkyl, phenyl, (phenyl)-lower alkyl, (halophenyl)-lower alkyl, ((lower-alkyl)phenyl)-lower-alkyl, ((lower-alkoxy)phenyl)-lower-alkyl, (naphthyl)-lower-alkyl, or (pyridyl)-lower-alkyl;

each R⁵ is, independently, hydrogen, halogen, trifluoromethyl, lower alkyl, unsubstituted or substituted phenyl, lower alkyl-thio, phenyl-lower alkyl-thio, lower alkyl-sulfonyl, or phenyl-lower alkyl-sulfonyl, OH, —(CH₂)_(m)—OR, —O—(CH₂)_(m)—OR⁸, —O—(CH₂)_(m)—NR⁷R¹⁰, —(CH₂)_(n)—NR⁷R⁷, —O—(CH₂)_(m)—NR⁷R¹⁰, —O—(CH₂)_(m)—NR⁷R⁷, —(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —(CH₂CH₂O)_(m)—R⁸, —O—(CH₂CH₂O)_(m)—R⁸, —(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —O—(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —(CH₂)—C(═O)NR⁷R¹⁰, —O—(CH₂)_(m)—C(═O)NR⁷R¹¹, —(CH₂)_(n)—(Z)_(g)—R⁷, —O—(CH₂)_(m)—(Z)_(g)—R⁷, —(CH₂)_(n)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —(CH₂)_(n)—CO₂R⁷, —O—(CH₂)_(m)—CO₂R⁷, —OSO₃H, —O-glucuronide, —O-glucose,

-Link-(CH₂)_(m)-CAP, -Link-(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂CH₂O)_(m)—CH₂-CAP, -Link-(CH₂CH₂O)_(m)—CH₂CH₂-CAP, -Link-(CH₂)_(m)—(Z)_(g)-CAP, -Link-(CH₂)_(n)(Z)_(g)—(CH₂)_(m)-CAP, -Link-(CH₂), —NR¹³—CH₂(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂)_(n)—(CHOR⁸)_(m)CH₂—NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(n)NR³—(CH₂)_(m)(CHOR⁸)_(n)CH₂NR¹³—(Z)_(g)-CAP, -Link-(CH₂)—(Z)_(g)(CH₂)_(m)-CAP, -Link-NH—C(═O)—NH—(CH₂)_(m)-CAP, -Link-(CH₂)_(m)—C(═O)NR¹³—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—(Z)_(g)—(CH₂)_(m)—(Z)_(g)-CAP, or -Link-Z—(CH₂)_(m)-Het-(CH₂)_(m)-CAP with the proviso that at least one R⁵ group contains at least one basic nitrogen;

The term —O-glucuronide, unless otherwise specified, means a group represented by

wherein the

O means the glycosidic linkage can be above or below the plane of the ring.

The term —O-glucose, unless otherwise specified, means a group represented by

wherein the

O means the glycosidic linkage can be above or below the plane of the ring.

In a preferred embodiment, R⁵ is one of the following:

hydrogen, halogen, trifluoromethyl, lower alkyl, unsubstituted or substituted phenyl, lower alkyl-thio, phenyl-lower alkyl-thio, lower alkyl-sulfonyl, or phenyl-lower alkyl-sulfonyl, OH, —(CH₂)_(m)—OR⁸, —O—(CH₂)_(m)—OR⁸, —(CH₂)_(n)—NR⁷R¹⁰, —O—(CH₂)_(m)—NR⁷R¹⁰, —(CH₂)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —(CH₂CH₂O)_(m)—R⁸, —O—(CH₂CH₂O)_(m)—R^(B), —(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —O—(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —(CH₂)_(n)—C(═O)NR⁷R¹⁰, —O—(CH₂)_(m)—C(═O)NR⁷R¹⁰, —(CH₂)_(n)—(Z)_(g)—R⁷, —O—(CH₂)_(m)—(Z)_(g)—R⁷, —(CH₂)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸), —CH₂OR⁸, —(CH₂)_(n)—CO₂R⁷, —O—(CH₂)_(m)—CO₂R⁷, —OSO₃H, —O-glucuronide, —O-glucose,

In a preferred embodiment, each —(CH₂)—(Z)_(g)—R⁷ falls within the scope of the structures described above and is, independently, —(CH₂)_(n)—NH—C(═NH)NH₂,

In another a preferred embodiment, each —O—(CH₂)—(Z)_(g)—R⁷ falls within the scope of the structures described above and is, independently, —O—(CH₂)_(m)—NH—C(═NH)—N(R⁷)₂, or —O—(CH₂)_(m)—CHNH₂—CO₂NR⁷R¹⁰.

In another preferred embodiment, R⁵ is —OH, —O—(CH₂)_(m)(Z)_(g)R¹², -Het-(CH₂)_(m)—NH—C(═NR¹³)—NR¹³R¹³, -Het-(CH₂)_(n)—(Z)_(g)—(CH₂)_(m)NH—C(═NR¹³)—NR¹³R¹³, -Link-(CH₂)_(m)—(Z)_(g)—(CH₂)_(m)-CAP, Link-(CH₂)_(n)—CR¹¹R¹¹-CAP, -Het-(CH₂)_(m)—CONR¹³R¹³, —(CH₂)_(n)—NR¹²R¹², —O—(CH₂)_(m)NR¹¹R¹¹, —O—(CH₂)_(m)—N^(⊕)—(R¹¹)₃, —(CH₂)_(n)—(Z)_(g)—(CH₂)_(m)—NR¹⁰R¹⁰, -Het-(CH₂)_(m)—(Z)_(g)—NH—C(═NR¹³)—NR¹³R¹³, —O—(CH₂)_(m)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)—C(═O)NR⁷R¹⁰, —O—(CH₂)_(m)—(Z)_(g)—R⁷, or —O—(CH₂)_(m)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸.

In a particularly preferred embodiment, R⁵ is -Link-(CH₂)_(m)-CAP, -Link-(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂CH₂O)_(m)—CH₂-CAP, -Link-(CH₂CH₂O)_(m)—CH₂CH₂-CAP, -Link-(CH₂)_(m)—(Z)_(g)-CAP, -Link-(CH₂)_(n)(Z)_(g)—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—NR¹³—CH₂(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂)_(n)—(CHOR⁸)_(m)CH₂—NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(n)NR¹³—(CH₂)_(m)(CHOR⁸)_(n)CH₂NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(m)—(Z)_(g)—(CH₂)_(m)-CAP, -Link-NH—C(═O)—NH—(CH₂)_(m)-CAP, -Link-(CH₂)_(m)—C(═O)NR¹³—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—(Z)_(g)—(CH₂)_(m)—(Z)_(g)-CAP, or -Link-Z_(g)—(CH₂)_(m)-Het-(CH₂)_(m)-CAP.

Each R¹⁴ is —C(═O)R⁷, -Amino Acid of the natural configuration; The term Amino Acid of the natural configuration shall mean the carbonyl of the amino acid is bonded to the Sulfur; so, for example, if the amino acid is alanine, the resulting —S—R¹⁴ structure is —S—(C═O)—CH(NH₂)—CH₃: if the amino acid is aspartic acid, the resulting —S—R¹⁴ is —S—(C═O)—CH(NH2)-CH₂—CO2H and so on throughout the twenty natural amino acids. Each R⁶ is, independently, hydrogen, —C(═O)—R⁷, or an Amino Acyl of the natural amino acid configuration;

In a preferred embodiment, R¹⁴ is H, isobutyrl, prpionyl, or 2-furoyl.

In a particularly preferred embodiment, R¹⁴ is acetyl.

In another preferred embodiment, R¹⁴ is —(C═O)—CHNH₂—(CH₂)₄NH₂.

Amino Acyl of the natural amino acid configuration refers to the twenty natural occurring amino acids comprised of glycine, alanine, valine, leucine, isoleucine, cysteine, methionine, phenylalanine, tyrosine, tryptophan, proline, serine, threonine, asparagine, glutamine, aspartic acid, glutamic acid, histidine, lysine, or arginine. For example, a structure of a compound of Formula I using R¹⁴=Amino Acyl of lysine is as follows:

Selected substituents within the compounds of the invention are present to a recursive degree. In this context, “recursive substituent” means that a substituent may recite another instance of itself. Because of the recursive nature of such substituents, theoretically, a large number of compounds may be present in any given embodiment. For example, R⁹ contains a R¹³ substituent. R¹³ can contain an R¹⁰ substituent and R¹⁰ can contain a R⁹ substituent. One of ordinary skill in the art of medicinal chemistry understands that the total number of such substituents is reasonably limited by the desired properties of the compound intended. Such properties include, by way of example and not limitation, physical properties such as molecular weight, solubility or log P, application properties such as activity against the intended target, and practical properties such as ease of synthesis.

By way of example and not limitation, R⁵, R¹³ and R¹⁰ are recursive substituents in certain embodiments. Typically, each of these may independently occur 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, 4, 3, 2, 1, or 0, times in a given embodiment. More typically, each of these may independently occur 12 or fewer times in a given embodiment. More typically yet, R⁹ will occur 0 to 8 times in a given embodiment, R¹³ will occur 0 to 6 times in a given embodiment and R¹⁰ will occur 0 to 6 times in a given embodiment. Even more typically yet, R⁹ will occur 0 to 6 times in a given embodiment, R¹³ will occur 0 to 4 times in a given embodiment and R¹⁰ will occur 0 to 4 times in a given embodiment.

Recursive substituents are an intended aspect of the invention. One of ordinary skill in the art of medicinal chemistry understands the versatility of such substituents. To the degree that recursive substituents are present in an embodiment of the invention, the total number will be determined as set forth above.

Each -Het- is, independently, —N(R⁷)—, —N(R¹⁰)—, —S—, —SO—, —SO₂—; —O—, —SO₂NH—, —NHSO₂—, —NR⁷CO—, —CONR⁷—, —N(R¹³)—, —SO₂NR¹³—, —NR¹³CO—, or —CONR¹³—. In a preferred embodiment, -Het- is —O—, —N(R⁷)—, or —N(R¹⁰)—. Most preferably, -Het- is —O—.

Each -Link- is, independently, —O—, —(CH₂)—, —O(CH₂)_(m)—, —NR¹³—C(O)—NR¹³—, —NR¹³—C(═O)—(CH₂)_(m)—, —C(═O)NR¹³—(CH₂)_(m), —(CH₂)_(n)—(Z)_(g)—(CH₂)_(n), —S—, —SO—, —SO₂—, —SO₂NR⁷—, —SO₂NR¹⁰—, or -Het-. In a preferred embodiment, -Link- is —O—, —(CH₂)_(n)—, —NR¹³—C(═O)—(CH₂)_(m)—, or —C(═O)NR¹³—(CH₂)_(m)—.

each CAP is, independently

In a preferred embodiment, CAP is

Each g is, independently, an integer from 1 to 6. Therefore, each g may be 1, 2, 3, 4, 5, or 6.

Each m is an integer from 1 to 7. Therefore, each m may be 1, 2, 3, 4, 5, 6, or 7.

Each n is an integer from 0 to 7. Therefore, each n may be 0, 1, 2, 3, 4, 5, 6, or 7.

Each Z is, independently, —(CHOH)—, —C(═O)—, —(CHNR⁷R¹⁰)—, —(C═NR¹⁰)—, —NR¹⁰—, —(CH₂)_(n)—, —(CHNR¹³R¹³)—, —(C═NR¹³)—, or —NR¹³—. As designated by (Z)_(g) in certain embodiments, Z may occur one, two, three, four, five or six times and each occurrence of Z is, independently, —(CHOH)—, —C(═O)—, —(CHNR⁷R¹⁰)—, —(C═NR¹⁰)—, —NR¹⁰—, —(CH₂)_(n)—, —(CHNR¹³R¹³)—, —(C═NR¹³)—, or —NR¹³—. Therefore, by way of example and not by way of limitation, (Z)_(g) can be —(CHOH)—(CHNR⁷R¹⁰)—, —(CHOH)—(CHNR⁷R¹⁰)—C(═O)—, —(CHOH)—(CHNR⁷R¹⁰)—C(═O)—(CH₂)_(n)—, —(CHOH)—(CHNR⁷R¹⁰)—C(═O)—(CH₂)_(n)—(CHNR¹³R¹³)—, —(CHOH)—(CHNR⁷R¹⁰)—C(═O)—(CH₂)_(n)—(CHNR¹³R¹³)—C(═O)—, and the like.

In any variable containing —CHOR⁸— or —CH₂OR⁸ groups, when any —CHOR⁸— or —CH₂OR⁸ groups are located 1,2- or 1,3- with respect to each other, the R⁸ groups may, optionally, be taken together to form a cyclic mono- or di-substituted 1,3-dioxane or 1,3-dioxolane.

The compounds described herein may be prepared and used as the free base. Alternatively, the compounds may be prepared and used as a pharmaceutically acceptable salt. Pharmaceutically acceptable salts are salts that retain or enhance the desired biological activity of the parent compound and do not impart undesired toxicological effects. Examples of such salts are (a) acid addition salts formed with inorganic acids, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; (b) salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, malonic acid, sulfosalicylic acid, glycolic acid, 2-hydroxy-3-naphthoate, pamoate, salicylic acid, stearic acid, phthalic acid, mandelic acid, lactic acid and the like; and (c) salts formed from elemental anions for example, chlorine, bromine, and iodine.

It is to be noted that all enantiomers, diastereomers, and racemic mixtures, tautomers, polymorphs, pseudopolymorphs and pharmaceutically acceptable salts of compounds within the scope of formulae I (Ia-Id) are embraced by the present invention. All mixtures of such enantiomers and diastereomers are within the scope of the present invention.

A compound of formula I and its pharmaceutically acceptable salts may exist as different polymorphs or pseudopolymorphs. As used herein, crystalline polymorphism means the ability of a crystalline compound to exist in different crystal structures. The crystalline polymorphism may result from differences in crystal packing (packing polymorphism) or differences in packing between different conformers of the same molecule (conformational polymorphism). As used herein, crystalline pseudopolymorphism means the ability of a hydrate or solvate of a compound to exist in different crystal structures. The pseudopolymorphs of the instant invention may exist due to differences in crystal packing (packing pseudopolymorphism) or due to differences in packing between different conformers of the same molecule (conformational pseudopolymorphism). The instant invention comprises all polymorphs and pseudopolymorphs of the compounds of formula I and their pharmaceutically acceptable salts.

A compound of formula I and its pharmaceutically acceptable salts may also exist as an amorphous solid. As used herein, an amorphous solid is a solid in which there is no long-range order of the positions of the atoms in the solid. This definition applies as well when the crystal size is two nanometers or less. Additives, including solvents, may be used to create the amorphous forms of the instant invention. The instant invention comprises all amorphous forms of the compounds of formula I and their pharmaceutically acceptable salts.

The compounds of formula I may exist in different tautomeric forms. One skilled in the art will recognize that amidines, amides, guanidines, ureas, thioureas, heterocycles and the like can exist in tautomeric forms. All possible tautomeric forms of the amidines, amides, guanidines, ureas, thioureas, heterocycles and the like of all of the embodiments of formula I are within the scope of the instant invention.

“Enantiomers” refer to two stereoisomers of a compound which are non-superimposable mirror images of one another.

Stereochemical definitions and conventions used herein generally follow S. P. Parker, Ed., McGraw-Hill Dictionary of Chemical Terms (1984) McGraw-Hill Book Company, New York; and Eliel, E. and Wilen, S., Stereochemistry of Organic Compounds (1994) John Wiley & Sons, Inc., New York. Many organic compounds exist in optically active forms, i.e., they have the ability to rotate the plane of plane-polarized light. In describing an optically active compound, the prefixes D and L or R and S are used to denote the absolute configuration of the molecule about its chiral center(s). The prefixes d and l, D and L, or (+) and (−) are employed to designate the sign of rotation of plane-polarized light by the compound, with S, (−), or 1 meaning that the compound is levorotatory while a compound prefixed with R, (+), or d is dextrorotatory. For a given chemical structure, these stereoisomers are identical except that they are mirror images of one another. A specific stereoisomer may also be referred to as an enantiomer, and a mixture of such isomers is often called an enantiomeric mixture. A 50:50 mixture of enantiomers is referred to as a racemic mixture or a racemate, which may occur where there has been no stereoselection or stereospecificity in a chemical reaction or process. The terms “racemic mixture” and “racemate” refer to an equimolar mixture of two enantiomeric species, devoid of optical activity.

A single stereoisomer, e.g. an enantiomer, substantially free of its stereoisomer may be obtained by resolution of the racemic mixture using a method such as formation of diastereomers using optically active resolving agents (“Stereochemistry of Carbon Compounds,” (1962) by E. L. Eliel, McGraw Hill; Lochmuller, C. H., (1975) J. Chromatogr., 113:(3) 283-302). Racemic mixtures of chiral compounds of the invention can be separated and isolated by any suitable method, including: (1) formation of ionic, diastereomeric salts with chiral compounds and separation by fractional crystallization or other methods, (2) formation of diastereomeric compounds with chiral derivatizing reagents, separation of the diastereomers, and conversion to the pure stereoisomers, and (3) separation of the substantially pure or enriched stereoisomers directly under chiral conditions.

“Diastereomer” refers to a stereoisomer with two or more centers of chirality and whose molecules are not mirror images of one another. Diastereomers have different physical properties, e.g. melting points, boiling points, spectral properties, and reactivities. Mixtures of diastereomers may separate under high resolution analytical procedures such as electrophoresis and chromatography.

Without being limited to any particular theory, it is believed that the compounds of formula I function in vivo as biological reducing. By blocking epithelial sodium channels present in mucosal surfaces the compounds of formula I reduce the absorption of water by the mucosal surfaces. This effect increases the volume of protective liquids on mucosal surfaces, rebalances the system, and thus treats disease.

The compounds described herein may be prepared and used as the free base. Alternatively, the compounds may be prepared and used as a pharmaceutically acceptable salt. Pharmaceutically acceptable salts are salts that retain or enhance the desired biological activity of the parent compound and do not impart undesired toxicological effects. Examples of such salts are (a) acid addition salts formed with inorganic acids, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; (b) salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, malonic acid, sulfosalicylic acid, glycolic acid, 2-hydroxy-3-naphthoate, pamoate, salicylic acid, stearic acid, phthalic acid, mandelic acid, lactic acid and the like; and (c) salts formed from elemental anions for example, chlorine, bromine, and iodine.

It is to be noted that all enantiomers, diastereomers, and racemic mixtures, tautomers, polymorphs, pseudopolymorphs and pharmaceutically acceptable salts of compounds within the scope of formulae (X are embraced by the present invention. All mixtures of such enantiomers and diastereomers are within the scope of the present invention.

A compound of formula I and its pharmaceutically acceptable salts may exist as different polymorphs or pseudopolymorphs. As used herein, crystalline polymorphism means the ability of a crystalline compound to exist in different crystal structures. The crystalline polymorphism may result from differences in crystal packing (packing polymorphism) or differences in packing between different conformers of the same molecule (conformational polymorphism). As used herein, crystalline pseudopolymorphism means the ability of a hydrate or solvate of a compound to exist in different crystal structures. The pseudopolymorphs of the instant invention may exist due to differences in crystal packing (packing pseudopolymorphism) or due to differences in packing between different conformers of the same molecule (conformational pseudopolymorphism). The instant invention comprises all polymorphs and pseudopolymorphs of the compounds of formula I and their pharmaceutically acceptable salts.

A compound of formula I and its pharmaceutically acceptable salts may also exist as an amorphous solid. As used herein, an amorphous solid is a solid in which there is no long-range order of the positions of the atoms in the solid. This definition applies as well when the crystal size is two nanometers or less. Additives, including solvents, may be used to create the amorphous forms of the instant invention. The instant invention comprises all amorphous forms of the compounds of formula I and their pharmaceutically acceptable salts.

The compounds of formula I may exist in different tautomeric forms. One skilled in the art will recognize that amidines, amides, guanidines, ureas, thioureas, heterocycles and the like can exist in tautomeric forms. All possible tautomeric forms of the amidines, amides, guanidines, ureas, thioureas, heterocycles and the like of all of the embodiments of formula I are within the scope of the instant invention.

“Enantiomers” refer to two stereoisomers of a compound which are non-superimposable mirror images of one another.

Stereochemical definitions and conventions used herein generally follow S. P. Parker, Ed., McGraw-Hill Dictionary of Chemical Terms (1984) McGraw-Hill Book Company, New York; and Eliel, E. and Wilen, S., Stereochemistry of Organic Compounds (1994) John Wiley & Sons, Inc., New York. Many organic compounds exist in optically active forms, i.e., they have the ability to rotate the plane of plane-polarized light. In describing an optically active compound, the prefixes D and L or R and S are used to denote the absolute configuration of the molecule about its chiral center(s). The prefixes d and 1, D and L, or (+) and (−) are employed to designate the sign of rotation of plane-polarized light by the compound, with S, (−), or 1 meaning that the compound is levorotatory while a compound prefixed with R, (+), or d is dextrorotatory. For a given chemical structure, these stereoisomers are identical except that they are mirror images of one another. A specific stereoisomer may also be referred to as an enantiomer, and a mixture of such isomers is often called an enantiomeric mixture. A 50:50 mixture of enantiomers is referred to as a racemic mixture or a racemate, which may occur where there has been no stereoselection or stereospecificity in a chemical reaction or process. The terms “racemic mixture” and “racemate” refer to an equimolar mixture of two enantiomeric species, devoid of optical activity.

A single stereoisomer, e.g. an enantiomer, substantially free of its stereoisomer may be obtained by resolution of the racemic mixture using a method such as formation of diastereomers using optically active resolving agents (“Stereochemistry of Carbon Compounds,” (1962) by E. L. Eliel, McGraw Hill; Lochmuller, C. H., (1975) J. Chromaogr., 113:(3) 283-302). Racemic mixtures of chiral compounds of the invention can be separated and isolated by any suitable method, including: (1) formation of ionic, diastereomeric salts with chiral compounds and separation by fractional crystallization or other methods, (2) formation of diastereomeric compounds with chiral derivatizing reagents, separation of the diastereomers, and conversion to the pure stereoisomers, and (3) separation of the substantially pure or enriched stereoisomers directly under chiral conditions.

“Diastereomer” refers to a stereoisomer with two or more centers of chirality and whose molecules are not mirror images of one another. Diastereomers have different physical properties, e.g. melting points, boiling points, spectral properties, and reactivities. Mixtures of diastereomers may separate under high resolution analytical procedures such as electrophoresis and chromatography.

Prodrugs of Dithiol Mucolytics:

Many modern drugs are discovered through high-throughput screening or combinatorial chemistry. These compounds often are selected for their high pharmacological efficacy but unintentionally have poor drug-like characteristics (e.g., solubility, bioavailability, stability). One strategy to overcome these physiochemical, biopharmaceutical, and pharmacokinetic limitations is to use a prodrug form of the compound, a molecule that is inactive until undergoing an enzymatic or chemical transformation in vivo. Depending on the type of modification, prodrugs can have key advantages over their active counterparts: 1) increased stability and shelf-life, 2) increased aqueous solubility, 3) improved bioavailability, 4) increased lipophilicity/permeability, and 5) improved parenteral administration.

Of the drugs approved worldwide, 5-7% can be classified as prodrugs. These drugs are classified into two categories, bioprecurser prodrugs or carrier-linked prodrugs. Bioprecurser prodrugs are converted into pharmacologically active drugs by metabolic or chemical transformation. Carrier-linked prodrugs have a promoiety that is covalently linked to an active parent molecule. This promoiety is released, usually by enzymatic hydrolysis, activating the parent molecule once delivered to the therapeutic location. Design of the prodrug moiety is usually based on the drug-like characteristics that need improvement in a particular molecule, the available functional groups that are amenable to a promoiety, and the targeted organ or tissue. In cases where the promoiety cannot be directly attached due to reasons such as steric hinderance, spacers or linkers are also added. In order to be well-tolerated, the promoiety should be non-immunogenic, stable until reaching the therapeutic tissue, and rapidly excreted from the body, once cleaved from the parent. Esters are one of the most commonly used promoieties, due to their ease of removal from the parent drug by ubiquitous esterases (e.g., acetylcholinesterases, butyrylcholinesterases, carboxylesterases, arlesterases), capability of increasing drug solubility by masking charge groups, such as carboxylic acids and phophates, and relatively simple synthesis. Some other common functional groups that are utilized as promoieties are: carbonates, carbamates, amides, phosphates, and oximes.

Prodrugs could be particularly useful as inhaled therapeutics for muco-obstructive respiratory diseases, such as chronic bronchitis (CB), including the most common lethal genetic form of chronic bronchitis, cystic fibrosis (CF). We also hypothesized that additional molecular features can improve tolerability and duration of action of the monothiol mucolytics.

Specifically, we developed mucolytic pro-drugs, by integrating enzymatically labile, thiol-capping groups. These pro-drug mucolytic agents are advantageous in that: 1) they are completely inactive, and therefore, protected from auto-oxidation in solution; 2) the thiol protecting groups render the compounds completely odorless; and 3) the molecules can be designed to alter the rate of activation in vivo and can, therefore, be used to slow compound activation and to extend the duration of pharmacological action.

We developed a series of mucolytic pro-drugs that are activated by common enzymes that are present in the extracellular milieu (e.g., nucleotidases, phosphatases, and esterases). As a proof-of-concept, we tested the reducing kinetics of the pro-drug compound 68 in the presence or absence of an activating esterase. Under the conditions tested, 68 alone does not reduce the disulfide bonds, whereas the parent molecule 76 fully reduces all available disulfides in <10 seconds. However, the addition of an enzyme, capable of enzymatically cleaving 68, produces a concentration dependent increase in reaction rates. Importantly, 68, 70a/b and 76 all reduce MUC5B in human mucus samples, with kinetics similar to what is predicted above, demonstrating that enzymatic activities required for activation are present in mucus.

As discussed above, the compounds used to prepare the compositions of the present invention may be in the form of a pharmaceutically acceptable free base. Because the free base of the compound is generally less soluble in aqueous solutions than the salt, free base compositions are employed to provide more sustained release of active agent to the lungs. An active agent present in the lungs in particulate form which has not dissolved into solution is not available to induce a physiological response, but serves as a depot of bioavailable drug which gradually dissolves into solution.

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The present invention also provides methods of treatment that take advantage of the properties of the compounds described herein as discussed above. Thus, subjects that may be treated by the methods of the present invention include, but are not limited to, patients afflicted with cystic fibrosis, asthma, primary ciliary dyskinesia, chronic bronchitis, bronchiectasis chronic obstructive airway disease, artificially ventilated patients, patients with acute pneumonia, etc. The present invention may be used to obtain a sputum sample from a patient by administering the active compounds to at least one lung of a patient, and then inducing or collecting a sputum sample from that patient. Typically, the invention will be administered to respiratory mucosal surfaces via aerosol (liquid or dry powders) or lavage.

Subjects that may be treated by the method of the present invention also include patients being administered supplemental oxygen nasally (a regimen that tends to dry the airway surfaces); patients afflicted with an allergic disease or response (e.g., an allergic response to pollen, dust, animal hair or particles, insects or insect particles, etc.) that affects nasal airway surfaces; patients afflicted with a bacterial infection e.g., staphylococcus infections such as Staphylococcus aureus infections, Hemophilus influenza infections, Streptococcus pneumoniae infections, Pseudomonas aeuriginosa infections, etc.) of the nasal airway surfaces; patients afflicted with an inflammatory disease that affects nasal airway surfaces; or patients afflicted with sinusitis (wherein the active agent or agents are administered to promote drainage of congested mucous secretions in the sinuses by administering an amount effective to promote drainage of congested fluid in the sinuses), or combined, Rhinosinusitis. The invention may be administered to rhino-signal surfaces by topical delivery, including aerosols and drops.

The present invention may be used to improve mucus clearance other than airway surfaces. Such other mucosal surfaces include gastrointestinal surfaces, oral surfaces, genito-urethral surfaces, and ocular surfaces or surfaces of the eye. For example, the active compounds of the present invention may be administered by any suitable means, including locally/topically, orally, or rectally, in an effective amount.

In another aspect, a post-exposure prophylactic treatment or therapeutic treatment method is provided for treating infection from an airborne pathogen comprising administering an effective amount of the compounds of formula (I) to the lungs of an individual in need of such treatment against infection from an airborne pathogen. The pathogens which may be protected against by the prophylactic post exposure, rescue and therapeutic treatment methods of the invention include any pathogens which may enter the body through the mouth, nose or nasal airways, thus proceeding into the lungs. Typically, the pathogens will be airborne pathogens, either naturally occurring or by aerosolization. The pathogens may be naturally occurring or may have been introduced into the environment intentionally after aerosolization or other method of introducing the pathogens into the environment. Many pathogens which are not naturally transmitted in the air have been or may be aerosolized for use in bioterrorism. The pathogens for which the treatment of the invention may be useful includes, but is not limited to, category A, B and C priority pathogens as set forth by the NIAID. These categories correspond generally to the lists compiled by the Centers for Disease Control and Prevention (CDC). As set up by the CDC, Category A agents are those that can be easily disseminated or transmitted person-to-person, cause high mortality, with potential for major public health impact. Category B agents are next in priority and include those that are moderately easy to disseminate and cause moderate morbidity and low mortality. Category C consists of emerging pathogens that could be engineered for mass dissemination in the future because of their availability, ease of production and dissemination and potential for high morbidity and mortality. Particular examples of these pathogens are anthrax and plague. Additional pathogens which may be protected against or the infection risk therefrom reduced include influenza viruses, rhinoviruses, adenoviruses and respiratory syncytial viruses, and the like. A further pathogen which may be protected against is the coronavirus which is believed to cause severe acute respiratory syndrome (SARS).

The present invention also relates to the use of mucolytic agents of Formula I, or a pharmaceutically acceptable salt thereof, for preventing, mitigating, and/or treating deterministic health effects to the respiratory tract caused by exposure to radiological materials, particularly respirable aerosols containing radionuclides from nuclear attacks, such as detonation of radiological dispersal devices (RDD), or accidents, such as nuclear power plant disasters. As such, provided herein is a method for preventing, mitigating, and/or treating deterministic health effects to the respiratory tract and/or other bodily organs caused by respirable aerosols containing radionuclides in a recipient in need thereof, including in a human in need thereof, said method comprising administering to said human an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

A major concern associated with consequence management planning for exposures of members of the public to respirable aerosols containing radionuclides from nuclear attacks, such as detonation of radiological dispersal devices (RDD), or accidents, such as nuclear power plant disasters is how to prevent, mitigate or treat potential deterministic health effects to the respiratory tract, primarily the lung. It is necessary to have drugs, techniques and procedures, and trained personnel prepared to manage and treat such highly internally contaminated individuals.

Research has been conducted to determine ways in which to prevent, mitigate or treat potential damage to the respiratory tract and various organs in the body that is caused by internally deposited radionuclides. To date, most of the research attention has focused on strategies designed to mitigate health effects from internally deposited radionuclides by accelerating their excretion or removal. These strategies have focused on soluble chemical forms that are capable of reaching the blood stream and are deposited at remote systemic sites specific to a given radioelement. Such approaches will not work in cases where the deposited radionuclide is in relatively insoluble form. Studies have shown that many, if not most of the physicochemical forms of dispersed radionuclides from RDDs, will be in relatively insoluble form.

The only method known to effectively reduce the radiation dose to the lungs from inhaled insoluble radioactive aerosols is bronchoalveolar lavage or BAL. This technique, which was adapted from that already in use for the treatment of patients with alveolar proteinosis, has been shown to be a safe, repeatable procedure, even when performed over an extended period of time. Although there are variations in procedure, the basic method for BAL is to anaesthetize the subject, followed by the slow introduction of isotonic saline into a single lobe of the lung until the function residual capacity is reached. Additional volumes are then added and drained by gravity.

The results of studies using BAL on animals indicate that about 40% of the deep lung content can be removed by a reasonable sequence of BALs. In some studies, there was considerable variability among animals in the amount of radionuclide recovered. The reasons for the variability are currently not understood.

Further, based on a study on animals, it is believed that a significant dose reduction from BAL therapy results in mitigation of health effects due to inhalation of insoluble radionuclides.

In the study, adult dogs inhaled insoluble ¹⁴⁴Ce-FAP particles. Two groups of dogs were given lung contents of ¹⁴⁴Ce known to cause radiation pneumonitis and pulmonary fibrosis (about 2 MBq/kg body mass), with one group being treated with 10 unilateral lavages between 2 and 56 days after exposure, the other untreated. A third group was exposed at a level of ¹⁴⁴Ce comparable to that seen in the BAL-treated group after treatment (about 1 MBq/kg), but these animals were untreated. All animals were allowed to live their lifespans, which extended to 16 years. Because there is variability in initial lung content of ¹⁴⁴Ce among the dogs in each group, the dose rates and cumulative doses for each group overlap. Nevertheless, the effect of BAL in reducing the risk from pneumonitis/fibrosis was evident from the survival curves. In the untreated dogs with lung contents of 1.5-2.5 MBq/kg, the mean survival time was 370±65 d. For the treated dogs, the mean survival was 1270±240 d, which was statistically significantly different. The third group, which received lung contents of ¹⁴⁴Ce of 0.6-1.4 MBq had a mean survival time of 1800±230, which was not statistically different from the treated group. Equally important to the increased survival, the dogs in the high-dose untreated group died from deterministic effects to lung (pneumonitis/fibrosis) while the treated dogs did not. Instead, the treated dogs, like the dogs in the low-dose untreated group, mostly had lung tumors (hemangiosarcoma or carcinoma). Therefore, the reduction in dose resulting from BAL treatment appears to have produced biological effects in lung that were predictable based on the radiation doses that the lungs received.

Based on these results, it is believed that decreasing the residual radiological dose further by any method or combination of methods for enhancing the clearance of particles from the lung would further decrease the probability of health effects to lung. However, BAL is a procedure that has many drawbacks. BAL is a highly invasive procedure that must be performed at specialized medical centers by trained pulmonologists. As such, a BAL procedure is expensive. Given the drawbacks of BAL, it is not a treatment option that would be readily and immediately available to persons in need of accelerated removal of radioactive particles, for example, in the event of a nuclear attack. In the event of a nuclear attack or a nuclear accident, immediate and relatively easily administered treatment for persons who have been exposed or who are at risk of being exposed is needed. Sodium channel blockers administered as an inhalation aerosol have been shown to restore hydration of airway surfaces. Such hydration of airway surfaces aids in clearing accumulated mucus secretions and associated particulate matter from the lung. As such, without being bound by any particular theory, it is believed that sodium channel blockers can be used in combination with mucolytic agents described in this invention to accelerate the removal of radioactive particles from airway passages.

As discussed above, the greatest risk to the lungs following a radiological attack, such as a dirty bomb, results from the inhalation and retention of insoluble radioactive particles. As a result of radioactive particle retention, the cumulative exposure to the lung is significantly increased, ultimately resulting in pulmonary fibrosis/pneumonitis and potentially death. Insoluble particles cannot be systemically cleared by chelating agents because these particles are not in solution. To date, the physical removal of particulate matter through BAL is the only therapeutic regimen shown to be effective at mitigating radiation-induced lung disease. As discussed above, BAL is not a realistic treatment solution for reducing the effects of radioactive particles that have been inhaled into the body. As such, it is desirable to provide a therapeutic regimen that effectively aids in clearing radioactive particles from airway passages and that, unlike BAL, is relatively simple to administer and scalable in a large-scale radiation exposure scenario. In addition, it is also desirable that the therapeutic regimen be readily available to a number of people in a relatively short period of time.

In an aspect of the present invention, a method for preventing, mitigating, and/or treating deterministic health effects to the respiratory tract and/or other bodily organs caused by respirable aerosols containing radionuclides comprises administering an effective amount of a mucolytic agent of Formula I or a pharmaceutically acceptable salt thereof to an individual in need. In a feature of this aspect, the mucolytic agent is administered in conjunction with an osmolyte. With further regard to this feature, the osmolyte is hypertonic saline. In a further feature, the mucolytic agent and the osmolyte are administered in conjunction with an ion transport modulator. With further regard to this feature, the ion transport modulator may be selected from the group consisting of β-agonists, CFTR potentiators, purinergic receptor agonists, lubiprostones, and protease inhibitors. In another feature of this aspect, the radionuclides are selected from the group consisting of Cobalt-60, Cesium-137, Iridium-192, Radium-226, Phosphorus-32, Strontium-89 and 90, Iodine-125, Thallium-201, Lead-210, Thorium-234, Uranium-238, Plutonium, Cobalt-58, Chromium-51, Americium, and Curium. In a further feature, the radionuclides are from a radioactive disposal device. In yet another feature, the mucolytic agent or pharmaceutically acceptable salt thereof is administered in an aerosol suspension of respirable particles which the individual inhales. In an additional feature, the mucolytic agent or a pharmaceutically acceptable salt thereof is administered post-exposure to the radionuclides.

The present invention is concerned primarily with the treatment of human subjects, but may also be employed for the treatment of other mammalian subjects, such as dogs and cats, for veterinary purposes.

Another aspect of the present invention is a pharmaceutical composition, comprising a compound of formula I in a pharmaceutically acceptable carrier (e.g., an aqueous carrier solution). In general, the compound of formula I is included in the composition in an amount effective to reduce the viscosity of mucus on mucosal surfaces.

An aspect of the present invention is the combination of prodrug mucolytic agents with other drugs or excipients to improve the efficacy and tolerability of the compounds described in this invention.

Another aspect of the present invention is administering potent prodrug reducing agents in combination with osmolytes. A simple means to restore airway surface hydration in subjects with muco-obstructive diseases is to inhale hypertonic osmolyte solutions (most frequently 7% hypertonic saline (HS)), which draws water onto the airway surface. Rehydration of the lubricant periciliary layer (PCL) of the airway surface facilitates mucus clearance and, therefore, the removal of inhaled infectious agents.

Inhaled HS is a unique therapeutic agent as it is used by ˜60% of CF patients nationwide, but is not FDA approved for daily use for pulmonary disease. As such, HS has not undergone the rigorous clinical testing to identify the dose and dosing frequency that are most efficacious and well tolerated. Instead, the HS regime has been optimized in practice by patients and physicians. Most commonly, HS is administered as two 15 minute inhalation treatments of 4 mL of 7% hypertonic saline per treatment. The tonicity of HS used by patients (7% NaCl) has been identified as a maximum concentration that is generally tolerated (i.e. minimal irritation or bronchoconstriction).

Another approach to replenish the protective liquid layer on mucosal surfaces is to “re-balance” the system by blocking Na⁺ channel and liquid absorption. The epithelial protein that mediates the rate-limiting step of Na⁺ and liquid absorption is the epithelial Na⁺ channel (ENaC). ENaC is positioned on the apical surface of the epithelium, i.e. the mucosal surface-environmental interface. Other approaches to hydrate the airway surface include chloride (Cl⁻) secretogogues that draw Cl⁻ and water into the ASL.

The compounds of Formula I may also be used in conjunction with osmolytes thus lowering the dose of the compound needed to hydrate mucosal surfaces. This important property means that the compound will have a lower tendency to cause undesired side-effects. Active osmolytes of the present invention are molecules or compounds that are osmotically active (i.e., are “osmolytes”). “Osmotically active” compounds of the present invention are membrane-impermeable (i.e., essentially non-absorbable) on the airway or pulmonary epithelial surface. The terms “airway surface” and “pulmonary surface,” as used herein, include pulmonary airway surfaces such as the bronchi and bronchioles, alveolar surfaces, and nasal and sinus surfaces. Active compounds of the present invention may be ionic osmolytes (i.e., salts), or may be non-ionic osmolytes (i.e., sugars, sugar alcohols, and organic osmolytes). It is specifically intended that both racemic forms of the active compounds that are racemic in nature are included in the group of active compounds that are useful in the present invention. It is to be noted that all racemates, enantiomers, diastereomers, tautomers, polymorphs and pseudopolymorphs and racemic mixtures of the osmotically active compounds are embraced by the present invention.

Active compounds of the present invention may be ionic osmolytes (i.e., salts), or may be non-ionic osmolytes (i.e., sugars, sugar alcohols, and organic osmolytes). It is specifically intended that both racemic forms of the active compounds that are racemic in nature are included in the group of active compounds that are useful in the present invention. It is to be noted that all racemates, enantiomers, diastereomers, tautomers, polymorphs and pseudopolymorphs and racemic mixtures of the osmotically active compounds are embraced by the present invention.

Active osmolytes useful in the present invention that are ionic osmolytes include any salt of a pharmaceutically acceptable anion and a pharmaceutically acceptable cation. Preferably, either (or both) of the anion and cation are non-absorbable (i.e., osmotically active and not subject to rapid active transport) in relation to the airway surfaces to which they are administered. Such compounds include but are not limited to anions and cations that are contained in FDA approved commercially marketed salts, see, e.g., Remington: The Science and Practice of Pharmacy, Vol. II, pg. 1457 (19.sup.th Ed. 1995), incorporated herein by reference, and can be used in any combination including their conventional combinations.

Pharmaceutically acceptable osmotically active anions that can be used to carry out the present invention include, but are not limited to, acetate, benzenesulfonate, benzoate, bicarbonate, bitartrate, bromide, calcium edetate, camsylate (camphorsulfonate), carbonate, chloride, citrate, dihydrochloride, edetate, edisylate (1,2-ethanedisulfonate), estolate (lauryl sulfate), esylate (1,2-ethanedisulfonate), fumarate, gluceptate, gluconate, glutamate, glycollylarsanilate (p-glycollamidophenylarsonate), hexylresorcinate, hydrabamine (N,N′-Di(dehydroabietyl)ethylenediamine), hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isethionate, lactate, lactobionate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate, nitrte, pamoate (embonate), pantothenate, phosphate or diphosphate, polygalacturonate, salicylate, stearate, subacetate, succinate, sulfate, tannate, tartrate, teoclate (8-chlorotheophyllinate), triethiodide, bicarbonate, etc. Particularly preferred anions include chloride sulfate, nitrate, gluconate, iodide, bicarbonate, bromide, and phosphate.

Pharmaceutically acceptable cations that can be used to carry out the present invention include, but are not limited to, organic cations such as benzathine (N,N′-dibenzylethylenediamine), chloroprocaine, choline, diethanolamine, ethylenediamine, meglumine (N-methyl D-glucamine), procaine, D-lysine, L-lysine, D-arginine, L-arginine, triethylammonium, N-methyl D-glycerol, and the like. Particularly preferred organic cations are 3-carbon, 4-carbon, 5-carbon and 6-carbon organic cations. Metallic cations useful in the practice of the present invention include but are not limited to aluminum, calcium, lithium, magnesium, potassium, sodium, zinc, iron, ammonium, and the like. Particularly preferred cations include sodium, potassium, choline, lithium, meglumine, D-lysine, ammonium, magnesium, and calcium.

Specific examples of osmotically active salts that may be used with the sodium channel blockers described herein to carry out the present invention include, but are not limited to, sodium chloride, potassium chloride, choline chloride, choline iodide, lithium chloride, meglumine chloride, L-lysine chloride, D-lysine chloride, ammonium chloride, potassium sulfate, potassium nitrate, potassium gluconate, potassium iodide, ferric chloride, ferrous chloride, potassium bromide, etc. Either a single salt or a combination of different osmotically active salts may be used to carry out the present invention. Combinations of different salts are preferred. When different salts are used, one of the anion or cation may be the same among the differing salts.

Osmotically active compounds of the present invention also include non-ionic osmolytes such as sugars, sugar-alcohols, and organic osmolytes. Sugars and sugar-alcohols useful in the practice of the present invention include but are not limited to 3-carbon sugars (e.g., glycerol, dihydroxyacetone); 4-carbon sugars (e.g., both the D and L forms of erythrose, threose, and erythrulose); 5-carbon sugars (e.g., both the D and L forms of ribose, arabinose, xylose, lyxose, psicose, fructose, sorbose, and tagatose); and 6-carbon sugars (e.g., both the D and L forms of altose, allose, glucose, mannose, gulose, idose, galactose, and talose, and the D and L forms of allo-heptulose, allo-hepulose, gluco-heptulose, manno-heptulose, gulo-heptulose, ido-heptulose, galacto-heptulose, talo-heptulose). Additional sugars useful in the practice of the present invention include raffinose, raffinose series oligosaccharides, and stachyose. Both the D and L forms of the reduced form of each sugar/sugar alcohol useful in the present invention are also active compounds within the scope of the invention. For example, glucose, when reduced, becomes sorbitol; within the scope of the invention, sorbitol and other reduced forms of sugar/sugar alcohols (e.g., mannitol, dulcitol, arabitol) are accordingly active compounds of the present invention.

Osmotically active compounds of the present invention additionally include the family of non-ionic osmolytes termed “organic osmolytes.” The term “organic osmolytes” is generally used to refer to molecules used to control intracellular osmolality in the kidney. See e.g., J. S. Handler et al., Comp. Biochem. Physiol, 117, 301-306 (1997); M. Burg, Am. J. Physiol. 268, F983-F996 (1995), each incorporated herein by reference. Although the inventor does not wish to be bound to any particular theory of the invention, it appears that these organic osmolytes are useful in controlling extracellular volume on the airway/pulmonary surface. Organic osmolytes useful as active compounds in the present invention include but are not limited to three major classes of compounds: polyols (polyhydric alcohols), methylamines, and amino acids. The polyol organic osmolytes considered useful in the practice of this invention include, but are not limited to, inositol, myo-inositol, and sorbitol. The methylamine organic osmolytes useful in the practice of the invention include, but are not limited to, choline, betaine, carnitine (L-, D- and DL forms), phosphorylcholine, lyso-phosphorylcholine, glycerophosphorylcholine, creatine, and creatine phosphate. The amino acid organic osmolytes of the invention include, but are not limited to, the D- and L-forms of glycine, alanine, glutamine, glutamate, aspartate, proline and taurine. Additional osmolytes useful in the practice of the invention include tihulose and sarcosine. Mammalian organic osmolytes are preferred, with human organic osmolytes being most preferred. However, certain organic osmolytes are of bacterial, yeast, and marine animal origin, and these compounds are also useful active compounds within the scope of the present invention.

Under certain circumstances, an osmolyte precursor may be administered to the subject; accordingly, these compounds are also useful in the practice of the invention. The term “osmolyte precursor” as used herein refers to a compound which is converted into an osmolyte by a metabolic step, either catabolic or anabolic. The osmolyte precursors of this invention include, but are not limited to, glucose, glucose polymers, glycerol, choline, phosphatidylcholine, lyso-phosphatidylcholine and inorganic phosphates, which are precursors of polyols and methylamines. Precursors of amino acid osmolytes within the scope of this invention include proteins, peptides, and polyamino acids, which are hydrolyzed to yield osmolyte amino acids, and metabolic precursors which can be converted into osmolyte amino acids by a metabolic step such as transamination. For example, a precursor of the amino acid glutamine is poly-L-glutamine, and a precursor of glutamate is poly-L-glutamic acid.

In one embodiment of this invention, mucolytic agents are utilized to provide access to other therapeutic agents through the mucus layer to the airway epithelium. Mucus forms a diffusion barrier which can prevent therapeutic molecules from reaching their intended site of action.

The access of the following therapeutic agents to their site of action in the airway epithelium could be enhanced by the pre- or co-treatment with the prodrug mucolytic agents described in this invention.

Sodium Channel Blockers:

Coordinated ion transport by the airway epithelia directly regulates the hydration level of the mucosal surface. Importantly, sodium absorption through the epithelial sodium channel (ENaC) provides the rate-limiting step in hydration. In human subjects with loss of function mutation in ENaC have ‘wet’ airway surfaces and extraordinarily fast mucous clearance (Kerem et al., N Engl J Med. 1999 Jul. 15; 341(3):156-62). Conversely, increased sodium absorption through ENaC has been shown to be the underlying cause of mucous dehydration and the formation of mucous plugs in the lungs CF patients. Furthermore, transgenic mice that overexpress ENaC in the lungs have dehydrated airway surfaces and reduced/absent mucous clearance that results in death (Hummler et al., Proc Natl Acad Sci USA. 1997 Oct. 14; 94(21):11710-5). As predicted from clinical and experimental data, pharmacological blockade of ENaC conserves liquid on airway surfaces and increases mucus clearance (Hirsh et al., J Pharmacol Exp Ther. 2008; 325(1):77-88). Particular examples include, but are not limited to:

Small Molecule Channel Blockers:

Small molecule ENaC blockers are capable of directly preventing sodium transport through the ENaC channel pore. ENaC blocker that can be administered by the methods of this invention include, but are not limited to, amiloride, benzamil, phenamil, and amiloride analogues as exemplified by U.S. Pat. Nos. 6,858,614, 6,858,615, 6,903,105, 6,995,160, 7,026,325, 7,030,117, 7,064,129, 7,186,833, 7,189,719, 7,192,958, 7,192,959, 7,241,766, 7,247,636, 7,247,637, 7,317,013, 7,332,496, 7,345,044, 7,368,447, 7,368,450, 7,368,451, 7,375,107, 7,399,766, 7,410,968, 7,820,678, 7,842,697, 7,868,010, 7,875,619. 7,956,059, 8,008,494, 8,022,210, 8,124,607, 8,143,256, 8,163,758, 8,198,286, 8,211,895, 8,324,218 8,507,497 8,575,176, 8,669,262, 7,956,059, 8,008,494, 8,022,210, 8,124,607, 8,143,256, 8,163,758, 8,198,286, 8,211,895, 8,324,218 8,507,497 8,575,176, 8,669,262, 7,956,059, 8,008,494, 8,022,210, U.S. Patent Application Publication No. US2014/0142118-A1, U. S. Patent Application No. US20140170244-A1, and U. S. Patent Application No. US20140171447-A1.

Protease Inhibitors:

ENaC proteolysis is well described to increase sodium transport through ENaC. Protease inhibitor block the activity of endogenous airway proteases, thereby preventing ENaC cleavage and activation. Protease that cleave ENaC include furin, meprin, matriptase, trypsin, channel associated proteases (CAPs), and neutrophil elastases. Protease inhibitors that can inhibit the proteolytic activity of these proteases that can be administered by the methods of this invention include, but are not limited to, camostat, prostasin, furin, aprotinin, leupeptin, and trypsin inhibitors.

Nucleic Acids and Small Interfering RNAs (siRNA):

Any suitable nucleic acid (or polynucleic acid) can be used to carry out the present invention, including but not limited to antisense oligonucleotide, siRNA, miRNA, miRNA mimic, antagomir, ribozyme, aptamer, and decoy oligonucleotide nucleic acids. See, e.g., US Patent Application Publication No. 20100316628. In general, such nucleic acids may be from 17 or 19 nucleotides in length, up to 23, 25 or 27 nucleotides in length, or more.

Any suitable siRNA active agent can be used to carry out the present invention. Examples include, but are not limited to, those described in U.S. Pat. No. 7,517,865 and US Patent Applications Nos. 20100215588; 20100316628; 20110008366; and 20110104255. In general, the siRNAs are from 17 or 19 nucleotides in length, up to 23, 25 or 27 nucleotides in length, or more.

Secretogogues:

Mutations in the cystic fibrosis (CF) gene result in abnormal ion transport across the respiratory epithelium (Matsui et al., Cell 1998; 95:1005-15). Excessive absorption of sodium and the inability to secrete chloride by the airway epithelium in patients with CF drives water absorption down an osmotic gradient generated by inappropriate salt absorption, dehydrating airway mucous secretions and reducing the volume of liquid in the PCL. In COPD, cigarette smoke impairs CFTR function, thus creating an acquired phenotype similar to CF.

P2Y₂ Receptor Agonists:

Agents that that may be administered in combination with the methods and molecules described in the present invention include a group of P2Y₂ agonists. Purinergic (P2Y₂) receptors are abundant on luminal surface of human bronchial epithelium (HBE) and are known to stimulate Cl⁻ secretion and inhibit Na⁺ absorption (Goralski et al., Curr Opin Pharmacol. 2010 June; 10(3):294-9). UTP is an example of an endogenous P2Y₂ receptor agonist that provides a robust stimulation of chloride secretion, inhibition of sodium absorption and increase in airway surface liquid layer in airway epithelium, thus increasing the mucus clearance which is the primary defense mechanism of the lung. Early studies using uridine-5-triphosphate (UTP) delivered via aerosol to airway surfaces of CF and primary cilia dyskinesia (PCD) patients suggested the usefulness of UTP in enhancing MC and improving mean cough clearance rates.

Suitable P2Y₂ receptor agonists are described in, but are not limited to, U.S. Pat. Nos. 6,264,975, 5,656,256, 5,292,498, 6,348,589, 6,818,629, 6,977,246, 7,223,744, 7,531,525 and U.S. Pat. AP.2009/0306009 each of which is incorporated herein by reference.

Activators of Alternative Chloride Channels Such as CaCCs and ClC-2 Class Channels:

CaCCs are broadly expressed in mammalian cells where they are involved in a wide range of physiological functions, including transepithelial fluid secretion, oocyte fertilization, olfactory and sensory signal transduction, smooth muscle contraction, and neuronal and cardiac excitation. Whole cell current analysis indicates several common features between CaCC subfamilies, including slow activation following membrane depolarization, outwardly rectifying steady state currents and greater iodide than chloride permeability. Single channel analysis has suggested four or more distinct CaCC subclasses, with a wide range of reported single channel conductances from less than 2 pS in cardiac myocytes to 50 pS in airway epithelial cells.

The consequences of CaCC activation are cell type specific, for example, chloride secretion in epithelial cells, action potential generation in olfactory receptor neurons, smooth muscle contraction, and prevention of polyspermia in oocytes. In some cell types, such as smooth muscle cells, membrane depolarization activates voltage gated calcium channels, increasing intracellular calcium concentration. Although CaCCs were functionally characterized nearly three decades ago, their molecular identity has remained unclear until recently, with potential candidates including bestrophins (BEST1-BEST4) (Sun et al., Proc Natl Acad Sci USA 99, 4008-4013 (2002) and Tsunenari et al., J Biol Chem 278, 41114-41125 (2003)), the calcium activated chloride channel ClCA family proteins (Gruber et al., Genomics 1998; 54:200-214) and ClC3 (Huang P et al. (2001) Regulation of human CLC-3 channels by multifunctional Ca2+/calmodulin-dependent protein kinase. JBC 276: 20093-100). Three independent laboratories have identified TMEM16A, also called anoctamin1, as a strong candidate for a CaCC (Yang Y D et al. (2008) TMEM16A confers receptor-activated calcium-dependent chloride conductance. Nature. 455: 1210-15; Caputo A et al. (2008) TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity. Science. 322: 590-4; Schroeder B C et al. (2008) Expression cloning of TMEM16A as a calcium-activated chloride channel subunit. Cell. 134: 1019-29). Three different strategies were used: database searching for membrane proteins with multiple transmembrane segments and unknown function (Yang Y D et al. (2008) TMEM16A confers receptor-activated calcium-dependent chloride conductance. Nature. 455: 1210-15), functional genomics following the observation that interleukin 4 (114) treated bronchial epithelial cells show increased CaCC activity (Caputo A et al. (2008) TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity. Science. 322: 590-4), and expression cloning using axolotl oocytes that do not have endogenous CaCC activity (Schroeder B C et al. (2008) Expression cloning of TMEM16A as a calcium-activated chloride channel subunit. Cell. 134: 1019-29). There is strong evidence to suggest TMEM16A is a key component of CaCC, including similarity to native CaCCs in its electrophysiological properties, appearance of CaCC currents in various transfected cell systems, reduction in CaCC currents following RNAi knockdown, and its tissue distribution. TMEM16A has eight putative transmembrane segments without domains evidently involved in calcium regulation.

ClC-2 is a ubiquitously expressed, inwardly rectifying chloride channel that is activated by cell swelling. ClC-2 was thought to be involved in cell volume regulation, but it has different biophysical characteristics from the volume sensitive chloride channels that have been characterized in many tissues. Suitable alternative chloride channel activators are described in U.S. Pat. Nos. 6,015,828, 6,159,969 and 7,253,295. The therapeutic efficacy of activators of Alternative Chloride Channels such as CaCCs and ClC-2 Class Channels can be enhanced by the administration of compounds and methods of this invention.

Modulators of CFTR Activity:

The hereditary lethal disease cystic fibrosis is caused mutations in the gene encoding CFTR protein, a cAMP activated chloride channel expressed in the airway epithelia. Various mutations in CFTR cause ion transport dysfunction by limiting the chloride ion secretion to the surface of the airway epithelium via CFTR and by dysregulation of sodium ion absorption, leading to excessive absorption of sodium cations. These defects in ion transport result in impaired hydration of airway surface liquid layer, decrease in mucus clearance and lead to progressive loss of lung function. Recently, it has been shown that CFTR functional defects are present in cigarette smoke exposed tissue, thus implying the role of CFTR dysfunction in COPD.

Over 1500 putative mutations have been described in CFTR, which can be divided into classes according to the molecular mechanism of the genetic defect (Rowe et al., Pulm Pharmacol Ther., 23(4):268-78 (2010)). An understanding of the biology of each of these mutations has led to therapeutic strategies based on the particular mutation type. Class I mutations include premature termination codons (PTCs, e.g. nonsense mutations) within the coding region of CFTR, which cause premature truncation of normal protein translation. These mutations are found in 10% of CF patients, but are particularly common in Ashkenazi Jews (75% of mutant CFTR alleles). Class II CFTR mutations include F508del CFTR, the most common mutation in humans (accounting for 75% of alleles and found in approximately 90% of CF patients). The deletion of phenylalanine at the 508 position causes CFTR to exhibit abnormal folding characterized by deficient stabilization by domain-domain interactions between the nucleotide binding domain 1 (NBD1) and the transmembrane domains. The misfolded protein is recognized by cellular chaperones within the endoplasmic reticulum (ER), directed to the proteasome, and rapidly degraded prior to reaching its active site at the cell surface. Because the cellular machinery responsible for the recognition and degradation of the misfolded protein is not 100% efficient, particular individuals exhibit low levels of surface expression of F508del CFTR, which may account for partial CFTR activity (and a more mild CF phenotype) observed in individuals homozygous for F508del CFTR, and could represent a population more amenable to protein repair. Even when at the cell surface, F508del CFTR exhibits reduced gating, suggesting that misfolded CFTR also exhibits reduced CFTR ion channel activity. Class III and IV CFTR mutations are characterized by full-length CFTR that reaches the cell surface but exhibit reduced ion transport activity owing to abnormal channel gating (Class III, e.g. G551D) or reduced conductivity of the ion channel pore (Class IV, e.g. R117H). Similarly, splicing mutants (Class V) and mutations within the C-terminus (Class VI) are also full length, but exhibit reduced activity owing to reduced numbers of active channels within the plasma membrane. Although the molecular basis of CFTR mutants is complex and as yet incomplete, the classification of CFTR mutants can be simplified into the therapeutically relevant groups based on the activity of agents in development. Both traditional and high-throughput drug discovery programs have resulted in discovery of novel compounds that address specific mutant CFTR alleles. These ‘CFTR modulators’ are pharmacological agents intended to repair the CFTR protein and are described in each section that follows.

Potentiators of cell-surface cystic fibrosis transmembrane conductance regulator CFTR mutation classes that result in dysfunctional CFTR that resides at the plasma membrane include Class III, IV, V, and VI mutations and represent potential targets for CFTR activators. G551D CFTR represents an archetype CFTR allele for this category of agents, as it exhibits normal surface expression and half-life, but confers a severe defect in channel gating owing to an amino acid substitution in the adenosine triphosphate (ATP) binding pocket within the nucleotide binding domains (Gregory, R. J. et al. (1991) Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2. MCB 11: 3886-93; Bompadre, S. G. et al. (2007) G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects. Gen Physiol. 129: 285-298). Flavonoids are well known activators of mutant CFTR and were among the first to be studied for beneficial effects in human individuals (including topical administration). Although agents such as genistein were affected by lack of efficacy in the nasal airway, more recent efforts have demonstrated activity of the flavonoid quercetin in the nose. However, flavonoid agents are challenged by poor solubility and systemic absorption, and are poor development candidates for inhaled therapeutics. More recent discovery strategies have focused on identification of compounds that ‘potentiate’ CFTR activity, restoring endogenous regulation (e.g. cyclic adenosine monosphosphate (cAMP)-dependent regulation) and ion transport without excessive, constitutive activation that may potentially be detrimental (such as excessive CFTR activation seen with certain diarrheal illnesses). Identification of agents of this type is amenable to high-throughput screening-based strategies to discover agents that activate mutant CFTR by measuring the effects on anion conductance in cell-based screening assays. A number of specific strategies have been used for screens of this sort, including chloride sensitive dyes, fluorescence resonance energy transfer-based analysis of membrane potential, and cell conductance of airway monolayers. Identification and characterization of small molecule potentiators of mutant CFTR have led to the development of agents with pronounced activity in vitro and in the clinic.

Significant effort has been directed toward the goal of correcting the folding of F508del CFTR, thus restoring ion channel activity to the misfolded protein. A diverse array of cellular targets have been explored, commensurate with the large number of proteins now known to interact with CFTR biogenesis. Agents such as 4-phenyl butyrate downregulate Hsc70 (or other cell chaperones) central to the folding process, and represent an early example of compounds tested in the clinic. Other more recent efforts have resulted from high-throughput library screens for chloride channel function following incubation of test compounds with F508del expressing cells. A number of these strategies have identified F508del correctors that may address cell biogenesis through chaperone pathways. Pharmacologic activity of such agents has also been reported to augment F508del CFTR half-life in the plasma membrane through altered surface recycling attributed to features of the cellular processing machinery or reduced endocytic trafficking. This class of agents may be potential drug development candidates if their safety in vivo is confirmed. Other compounds have been shown to directly interact with CFTR and may offer greater specificity than agents that alter general aspects of cell folding or cellular quality control. The global cellular response to misfolded protein may also represent a target. Histone deacetylases (HDAC) have far-ranging effects on gene expression, and specific members of the HDAC family are involved in the ER associated degradation pathway promoting degradation of F508del CFTR. Treatment of CF cells with HDAC inhibitors can modulate ER stress, and HDACs such as suberoylanilidehydroxamic acid, as well as siRNA-silencing of HDACs, increase levels of F508del CFTR in the cell membrane. The combination of approaches such as these reveal a number of potential pharmacologic agents for F508del correction. Additive or synergistic rescue of F508del CFTR using more than one such strategy may offer hope of achieving ion transport activity sufficient to confer a normal phenotype in CF respiratory epithelia.

Read-through of premature termination codons (PTCs) represents another exciting approach to address the underlying cause of CF, and many other genetic diseases caused by PTCs. Certain aminoglycosides and other agents have the capacity to interact with the eukaryotic rRNA within the ribosomal subunits. Although this interaction is much weaker than that seen in prokaryotes and is distinct from the primary cause of aminoglycoside toxicity in human individuals, it can modestly reduce the fidelity of eukaryotic translation by interrupting the normal proofreading function of the ribosome. Insertion of a near cognate amino acid at a premature stop codon allows protein translation to continue until one of several stop codons normally present at the end of the mRNA transcript is reached and properly utilized. The specificity of the strategy has been attributed to greater stop codon fidelity at the authentic end of mRNA and has been established in vitro by demonstrating no detectable elongation beyond native stop codons.

CFTR activity modulating compounds that can be administered in combination with the methods and molecules described in the present invention include, but are not limited to, compounds described in US 2009/0246137 A1, US 2009/0253736 A1, US 2010/0227888 A1, U.S. Pat. No. 7,645,789, US 2009/0246820 A1, US 2009/0221597 A1, US 2010/0184739 A1, US 2010/0130547 A1, US 2010/0168094 A1, U.S. Pat. Nos. 7,553,855, 7,772,259 B2, 7,405,233 B2, US 2009/0203752, and U.S. Pat. No. 7,499,570.

Anti-Infective Agents:

Chronic obstructive pulmonary diseases are accompanied by both acute and chronic bacterial infections. Both acute and chronic infections lead to chronic inflammation that has acute flare-ups in the form of pulmonary exacerbations. The underlying inflammation is treated with variety of inhaled anti-inflammatory agents. For example, in cystic fibrosis the most common bacteria causing chronic infection is Pseudomonas aeruginosa (P. aeruginosa) and antibiotics that are effective against this bacteria are a major component of treatment (Flume, Am J Respir Crit Care Med. 176(10):957-69 (2007)). Also bacteria such as Staphylococcus aureus (S. aureus), Burkholderia cepacia (B. cepacia) and other gram negative organisms as well as anaerobes are isolated from respiratory secretions and people with CF may benefit from treatment of these pathogens to maintain their lung health. Anaerobic bacteria are also recognized as a feature of CF airways, sinuses in subjects with chronic sinusitis, and likely airways of subjects with COPD. Similarly, aspirations or microaspirations, especially in elderly population and during sleep, are associated with a chemical pneumonitis, anaerobic infections and subsequent bronchiectasis. An ideal treatment of aspiration-related pneumonitis and anaerobic infection would be an immediate treatment. As such, antibiotics are used to eradicate early infections, during pulmonary exacerbations and as chronic suppressive therapy.

The primary measure of antibiotic activity is the minimum inhibitory concentration (MIC). The MIC is the lowest concentration of an antibiotic that completely inhibits the growth of a microorganism in vitro. While the MIC is a good indicator of the potency of an antibiotic, it indicates nothing about the time course of antimicrobial activity. PK parameters quantify the lung tissue level time course of an antibiotic. The three pharmacokinetic parameters that are most important for evaluating antibiotic efficacy are the peak tissue level (Cmax), the trough level (Cmin), and the Area Under the tissue concentration time Curve (AUC). While these parameters quantify the tissue level time course, they do not describe the killing activity of an antibiotic. Integrating the PK parameters with the MIC gives us three PK/PD parameters which quantify the activity of an antibiotic: the Peak/MIC ratio, the T>MIC, and the 24 h-AUC/MIC ratio. The Peak/MIC ratio is simply the Cpmax divided by the MIC. The T>MIC (time above MIC) is the percentage of a dosage interval in which the serum level exceeds the MIC. The 24 h-AUC/MIC ratio is determined by dividing the 24-hour-AUC by the MIC. The three pharmacodynamic properties of antibiotics that best describe killing activity are time-dependence, concentration-dependence, and persistent effects. The rate of killing is determined by either the length of time necessary to kill (time-dependent), or the effect of increasing concentrations (concentration-dependent). Persistent effects include the Post-Antibiotic Effect (PAE). PAE is the persistent suppression of bacterial growth following antibiotic exposure.

Using these parameters, antibiotics can be divided into 3 categories:

PK/PD Pattern of Activity Antibiotics Goal of Therapy Parameter Type I Aminoglycosides Maximize 24 h- Concentration- Daptomycin concentrations AUC/MIC dependent killing Fluoroquinolones Peak/MIC and Prolonged Ketolides persistent effects Type II Carbapenems Maximize duration T > MIC Time-dependent Cephalosporins of exposure killing and Erythromycin Minimal persistent Linezolid effects Penicillins Type III Azithromycin Maximize 24 h- Time-dependent Clindamycin amount of drug AUC/MIC killing and Oxazolidinones Moderate to Tetracyclines prolonged persistent Vancomycin effects.

For Type I antibiotics (AG's, fluoroquinolones, daptomycin and the ketolides), the ideal dosing regimen would maximize concentration, because the higher the concentration, the more extensive and the faster is the degree of killing. Therefore, the 24 h-AUC/MIC ratio, and the Peak/MIC ratio are important predictors of antibiotic efficacy. For aminoglycosides, it is best to have a Peak/MIC ratio of at least 8-10 to prevent resistance. For fluoroquinolonesvs gram negative bacteria, the optimal 24 h-AUC/MIC ratio is approximately 125. Versus gram positives, 40 appears to be optimal. However, the ideal 24 h-AUC/MIC ratio for FQ's varies widely in the literature.

Type II antibiotics (beta-lactams, clindamycin, erythromcyin, carbapenems and linezolid) demonstrate the complete opposite properties. The ideal dosing regimen for these antibiotics maximizes the duration of exposure. The T>MIC is the parameter that best correlates with efficacy. For beta-lactams and erythromycin, maximum killing is seen when the time above MIC is at least 70% of the dosing interval.

Type III antibiotics (vancomycin, tetracyclines, azithromycin, and the dalfopristin-quinupristin combination) have mixed properties, they have time-dependent killing and moderate persistent effects. The ideal dosing regimen for these antibiotics maximizes the amount of drug received. Therefore, the 24 h-AUC/MIC ratio is the parameter that correlates with efficacy. For vancomycin, a 24 h-AUC/MIC ratio of at least 125 is necessary.

Patients including, but not limited to, CF, COPD, non-CF bronchiectasis, aspiration pneumonia, asthma and VAP patients suffering from respiratory infection caused by bacteria susceptible to meropenem may benefit from such treatment. Examples of carbapenam antibiotics are: imipenam, panipenam, meropenam, doripenem, biapenam, MK-826, DA-1131, ER-35786, lenapenam, S-4661, CS-834 (prodrug of R-95867), KR-21056 (prodrug of KR-21012), L-084 (prodrug of LJC 11036) and CXA-101. The therapeutic efficacy of all antiinfective agents described can be enhanced by the pre- or co-administration of compounds and methods of this invention.

Exemplary Anti-Inflammatory Agents:

Inhaled corticosteroids are the standard of chronic care for asthma, COPD and other respiratory diseases characterized by acute and chronic inflammation leading to airflow limitation. Examples of anti-inflammatory agents suitable for administration in combination with the methods and molecules described in the present invention include beclomethasone, budesonide, and fluticasone and a group of anti-inflammatory medications that do not contain steroids known as non-steroiodal anti-inflammatory drugs (NSAIDs).

Products of arachidonic acid metabolism, specifically the leukotrienes (LTs), contribute to pulmonary inflammation. Cysteinylleukotrienes (LTC4, LTD4, and LTE4) are produced predominantly by eosinophils, mast cells, and macrophages. Examples of leukotriene modifiers suitable for administration by the method of this invention include monteleukast, zileuton and zafirlukast.

Mast cell stabilizers are cromone medications such as cromolyn (sodium cromoglycate) used to prevent or control certain allergic disorders. They block a calcium channel essential for mast cell degranulation, stabilizing the cell and thereby preventing the release of histamine and related mediators. As inhalers they are used to treat asthma, as nasal sprays to treat hay fever (allergic rhinitis) and as eye drops for allergic conjunctivitis. Finally, in oral form they are used to treat the rare condition of mastocytosis.

PDE4 inhibitors have been shown to modulate pulmonary inflammation and used for treatment of chronic obstructive pulmonary diseases. Examples of PDE4 inhibitors suitable for use in combination with the methods and molecules described in the present invention include, but is not limited to theophylline and roflumilast.

Exemplary Bronchodilators:

Nitric Oxide (NO) Donors:

NO, NO Donors, NO and Peroxynitrite Scavengers and Inducible NO Synthase Activity Modulators. Nitric oxide is a potent endogenous vasodilator and bronchodilator that can be exogenously administered via inhalation. It is synthesized by the conversion of the terminal guanidine nitrogen atom of L-arginine via endothelial cell calcium dependent enzyme nitric oxide synthetase and then diffuses across the cell membrane to activate the enzyme guanylatecyclase. This enzyme enhances the synthesis of cyclic guanosine monophosphate (cGMP), causing relaxation of vascular and bronchial smooth muscle and vasodilatation of blood vessels (Palmer, Circ Res., 82(8):852-61 (1998)).

Nitric oxide synthesised in endothelial cells that line blood vessels has a wide range of functions that are vital for maintaining a healthy respiratory and cardiovascular systems (Megson I L et al Expert Opin Investig Drugs. 2002 May; 11(5):587-601.). Reduced nitric oxide availability is implicated in the initiation and progression of many diseases and delivery of supplementary nitric oxide to help prevent disease progression is an attractive therapeutic option. Nitric oxide donor drugs represent a useful means of systemic nitric oxide delivery and organic nitrates have been used for many years as effective therapies for symptomatic relief from angina. However, nitrates have limitations and a number of alternative nitric oxide donor classes have emerged since the discovery that nitric oxide is a crucial biological mediator.

In the respiratory tract, NO is produced by residential and inflammatory cells (Ricciardolo F L et al. Curr Drug Targets 2006 June; 7(6):721-35). NO is generated via oxidation of L-arginine that is catalysed by the enzyme NO synthase (NOS). NOS exists in three distinct isoforms: neuronal NOS (nNOS), inducible NOS (iNOS), and endothelial NOS (eNOS). NO derived from the constitutive isoforms of NOS (nNOS and eNOS) and other NO-adduct molecules (nitrosothiols) are able to modulate bronchomotor tone. NO derived from the inducible isoform of NO synthase, up-regulated by different cytokines via NF-kappaB-dependent pathway, seems to be a pro-inflammatory mediator with immunomodulatory effects. In aging CF patients, expression of iNOS is significantly reduced (Yoon et al., J Clin Invest. 2006 February; 116(2):436-46). This reduced expression of iNOS in chronic CF is associated with emergence of mucoid muc mutant subpopulation of P. aeruginosa. It has been suggested that 15 mM NO₂ ⁻kills mucA P. Aeruginosa in CF airways at pH 6.5. NO itself or as a precursor to iron-nitrosyl species has been implicated in this antimicrobial effect. Therefore inhaled NO₂ ⁻, including but not limited inhaled NaNO₂, has an appeal as a CF therapy. The production of NO under oxidative stress conditions secondarily generates strong oxidizing agents (reactive nitrogen species) that may amplify the inflammatory response in asthma and COPD. Moreover, NO can be exhaled and levels are abnormal in stable atopic asthma and during exacerbations in both asthma and COPD. Exhaled NO might therefore be a non-invasive tool to monitor the underlying inflammatory process. It is suggested that NOS regulation provides a novel target in the prevention and treatment of chronic inflammatory diseases of the airways such as asthma and COPD.

Examples of NO, NO donors and NO synthase activity modulators suitable for administration in combination with the methods and molecules described in the present invention include inhaled NO, agents disclosed in Vallance et al. Fundam Clin Pharmacol. 2003 February; 17(1):1-10, Al-Sa'doni H H et al. Mini Rev Med Chem. 2005 March; 5(3):247-54, Miller M R et al. Br J Pharmacol. 2007 June; 151(3):305-21. Epub 2007 Apr. 2 and Katsumi H et al. Cardiovasc Hematol Agents Med Chem. 2007 July; 5(3):204-8.

Under certain conditions, inducible NO synthase activity leads to overproduction of NO which in turn increases inflammation and tissue injury. Under these conditions, the following inducible NO synthase inhibitors, NO scavengers and peroxynitrite scavengers administered in combination with the methods and molecules described in the present invention are suitable: Bonnefous et al. J. Med. Chem., 2009, 52 (9), pp 3047-3062, Muscara et al AJP—GI June 1999 vol. 276 no. 6 G1313-G1316 or Hansel et al. FASEB Journal. 2003; 17:1298-1300.

Beta 2-Adrenergic Receptor Agonisis:

It has been established that administration of super-therapeutic concentrations of receptor agonists leads to receptor desensitization and loss of efficacy. For example, this phenomenon has been described for beta 2-adrenoceptor based bronchodilator agents (Duringer et al., Br J Pharmacol., 158(1):169-79 (2009)). High concentration of these receptor agonist agents leads to the receptor phosphorylation, internalization and potential degradation. Administration of receptor agonists, which cause tachyphylaxis following bolus administration via fast nebulizer, by inhalation over the course of 8 to 24 hours or overnight to a patient via nasal cannula improves the efficacy of such agents due to decreased extent of tachyphylaxis. Beta 2-adrenergic receptor agonsists include albuterol, levalbuterol, salbutamol, procaterol, terbutaline, pirbuterol, and metaproterenol. The therapeutic efficacy of beta 2-adrenergic receptor agonists can be enhanced by the pre- or co-administration of compounds and methods of this invention.

Exemplary Gene Carriers:

Examples of gene carriers for the administration of gene therapy include viruses, DNA:protein complexes, plasmids, DNAs, and RNAs.

Other Exemplary Therapeutic Agents:

Examples of other classes of therapeutic agents suitable for administration in combination with the methods and molecules described in the present invention include antivirals such as ribavirin, anti-fungal agents such as amphotericin, intraconazol and voriconazol, immunosuppressants, anti-rejection drugs such as cyclosporine, tacrolimus and sirolimus, bronchodilators including but not limited to anticholinergic agents such as ipratropium, tiotropium, aclidinium and others, PDE5 inhibitors siRNAs, gene therapy vectors, aptamers, endothelin-receptor antagonists, alpha-1-antitrypsin, prostacyclins, vaccines, PDE-4 and PDE-5 inhibitors and steroids such as beclamethasone, budesonide, ciclesonide, flunisolide, fluticasone, memetasone and triamcinolone.

EXPERIMENTAL PROCEDURES AND BIOLOGICAL ASSAYS Pro-Drug DTNB Assay

This assay was designed to determine whether prodrug caps added on to our dithiol mucolytic compounds can be cleaved from the molecule. If so, the outcome would be an “active” compound that is able to reduce the S—S bond in DTNB. When cleaved the resulting compound, NTB (2-nitro-5-thiobenzoate), is a colored product that can be measured spectrophotometrically at an absorbance of 412 nm (Abs₄₁₂). Using the molar extinction coefficient of NTB and measured maximum Abs₄₁₂, the molar amount of DTNB that reacted with our mucolytic agents can be calculated. Dithiol mucolytic compounds react at a 2:1 stoichiometric ratio with DTNB (i.e. 2 molecules of NTB are produced for every one molecule of a dithiol compound that is oxidized). Dithiol prodrugs were mixed at a final concentration of 22.5 μM with excess DTNB (100 μM final) in 1 mL 50 mM Tris-HCl buffer (pH 7.5) and maximum Abs₄₁₂ was measured. In the absence of a purified hydrolytic enzyme (e.g. porcine liver esterase; Sigma), the amount of DTNB cleavage observed is an indicator for stability of the cap on the prodrug compound (i.e. if the prodrug remains intact in solution the Abs₄₁₂=0). Next, 5 uL of esterase (bought as an ammonium sulfate suspension that is subsequently centrifuged to isolate the esterase and then dissolved in reaction buffer prior to assaying) is combined with excess DTNB (100 μM final) and 22.5 μM pro-drug in 1 mL 50 mM Tris-HCl buffer (pH 7.5). Cleavage of the prodrug cap can be visualized in real time via DTNB cleavage at Abs₄₁₂ by the esterase-liberated dithiol molecule.

Parallel Artificial Membrane Permeability (PAMPA) Assay:

This assay measures the permeability of small molecules across an artificial phospholipid membrane to help predict in vivo drug permeability. First, 500 μM stock solutions were made up in PBS and tested by the DTNB assay (described above) to determine compound activity concentrations. Next, 300 μL of the 500 μM compound stock solution and 200 uL PBS were added per well to the donor and acceptor plates, respectively (BD Gentest™ Pre-Coated PAMPA Plate System). The acceptor plate was then placed on top of the donor plate and allowed to incubate at room temperature for 5 hours. After incubation, the donor and acceptor plates were separated. For each reaction, samples were taken from both the acceptor and donor plates and were combined with DTNB prior to reading spectrophotometrically (maximum Abs₄₁₂). For prodrug samples, 1 μL of purified esterase (porcine liver esterase; Sigma) was added per well and the samples were incubated at room temperature for 5 minutes to allow for cleavage of the pro-drug cap prior to addition of DTNB. Using the concentrations of compound identified in both the donor and acceptor plates for each sample, a compound permeability parameter was calculated following equations outlined in the BD Gentest™ Pre-Coated PAMPA Plate System Manual.

Mucin Agarose Gel Western Blots:

This assay tests whether mucin has been reduced by mucolytic compounds. Various mucin-containing substrates (e.g. saliva, primary human bronchial epithelial (HBEs) cell mucus (either on cultures or harvested), and sputum) treated with our dithiol mucolytic compounds are quenched upon completion of the treatment period with a 10-fold excess of N-ethylmaleimide in order to alkylate any remaining active compound and to prevent further mucin reduction. A 10× concentrated sample loading buffer is diluted into each sample (lx TAE/5% glycerol/0.1% SDS/Bromophenol Blue). Samples (50 μg) were analyzed by electrophoresis on 0.9% agarose gels using a buffer system consisting of 1×TAE/0.1% SDS. The agarose gel was soaked for 15 min in 4×SSC (0.6 M NaCl, 60 mM Tri-sodium citrate dehydrate) containing 10 mM DTT before transferring the samples from the gel onto a nitrocellulose membrane by vacuum blotter. Unreduced and reduced Muc5B and Muc5AC were visualized on a LiCor Odyssey imaging detection system using a polyclonal antibody directed towards Muc5B.

HBE ADME Assay:

This assay was designed to determine if our dithiol prodrug compounds would be retained on the apical surface of human bronchial epithelial cells (HBE) (i.e. they are predominately cell impermeant) and if the compounds could be metabolized to their active forms (i.e. are there relevant hydrolytic enzymes present). Towards this goal, 15 μL of 10 mM dithiol prodrug compound was added to the apical surface of HBEs. At indicated time points, mucus from the apical surface was isolated with a PBS wash that contained 10-fold excess of N-ethylmaleimide in order to alkylate any remaining active compound and to prevent further mucin reduction. In addition the HBE cells and basolateral media were isolated at each time point. The form (e.g., prodrug, active metabolite, oxidized metabolite) and location (apical, cellular, basolateral media) of each compound was analyzed by LC-MS.

Compounds of Formula I:

Compounds of formula I are readily prepared by methods well known in the art as exemplified and detailed below.

General Procedure:

All reagent and solvents were purchased from Aldrich Chemical Corp. Chem-Impex International Inc. and TCI chemical industry Co. Ltd. NMR spectra were obtained on either a Bruker AC 400 (¹H NMR at 400 MHz) or a Bruker AC 300 (¹H NMR at 300 MHz). Solvents CDCl₃, CD₃OD and DMSO-d₆ were purchased from Aldrich or Cambridge Isotope Laboratories, unless otherwise specified. Chemical shifts are reported in ppm relative to tetramethylsilane (TMS) as the internal standard. Data is reported as follows: chemical shift, integration, multiplicity (s=singlet, d=doublet, t=triplet, q=quartet, br=broad, m=multiplet), and coupling constants (Hz). Flash chromatography was performed on a Combiflash system (Combiflash Rf, Teledyne Isco) charged with silica gel column (Redi Sep. Rf, Teledyne Isco) or reverse phase column (High performance C18 Gold column). ESI Mass spectra were obtained on a Shimadzu LCMS-2010 EV Mass Spectrometer. HPLC analyses were obtained using a Waters XTerra MS C18 5 μm 4.6×150 mm Analytical Column detected at 220 nm (unless otherwise specified) on a Shimadzu Prominence HPLC system. All reactions are monitored by TLC and LCMS and for polar compound reactions are monitored by HPLC and LCMS analysis.

1. Preparation of of S,S′-((4,5-bis(2-((S)-2,6-diaminohexanamido)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride 11

Preparation of 5,6-dimethoxyisobenzofuaran-1(3H)-one (2)

HCl gas was bubbled through an aqueous formaldehyde (37%, 70 mL) at 0° C. and then at rt to get a saturated solution (1.5 h). This solution was charged with 3,4-dimethoxybenzoic acid 1 (9.00 g, 49.5 mmol) portionwise. The mixture was warmed to 70° C. and stirred at that temperature for 7 h; HCl gas was continuously bubbled through the solution during this period of time. The reaction mixture was stirred at room temperature for 16 h. The solvent was removed, water (100 mL) was added, and the mixture was neutralized with aqueous NH₄OH solution. A solid formed, which was filtered and washed with water. Recrystallization of the product from ethanol yielded a brown solid (5.00 g, 52%). Additionally 2.0 g of impure 2 was isolated as well.

Alternative preparation of 5,6-dimethoxyisobenzofuran-1(3H)-one (2)

Concentrated HCl (37%, 150 mL) was added to 3,4-dimethoxybenzoic acid 1 (10.0 g, 54.9 mmol), followed by aqueous formaldehyde (37%, 75 mL). The mixture was warmed to 90° C. and stirred at that temperature for 5 h. The solvent was removed and the residue was portioned between water (100 mL) and EtOAc (250 ml). The organic layer was separated and the aqueous layer was extracted with EtOAc (3×200 mL). The combined organic layers were washed with 2.5 M NaOH, followed by water, and concentrated. The residue was purified by column chromatography (silica gel, 25 to 50% EtOAc in hexanes) to afford compound 2 (7.00 g, 66%) as an off-white solid: ¹H NMR (400 MHz, DMSO-d₆) δ 7.26 (s, 1H), 7.23 (s, 1H), 5.27 (s, 2H), 3.87 (s, 3H), 3.84 (s, 3H).

Preparation of 5,6-dihydroxyisobenzofuran-1(3H)-one (3)

A solution of compound 2 (7.00 g, 36.1 mmol) in CH₂Cl₂ (150 mL) was cooled to −78° C. and BBr₃ (8.52 mL, 90.2 mmol) was added at the same temperature. Stirring was continued at −78° C. for 30 min, and the reaction mixture was brought to rt and stirred for 16 h. The reaction mixture was quenched with MeOH at 0° C. and then the solvent was removed. The residue was partition between water (100 mL) and EtOAc (200 mL); the EtOAc layer was separated. The aqueous layer was extracted with EtOAc (3×200 mL). The combined organic layers were concentrated and the residue was purified by column chromatography (silica gel, 40-60% EtOAc in hexanes) to afford compound 3 (5.00 g, 83%) as an off-white solid: ¹H NMR (400 MHz, DMSO-d₆) δ 10.18 (br s, 1H), 9.65 (br s, 1H), 7.06 (s, 1H), 6.92 (s, 1H), 5.16 (s, 2H).

Preparation of di-tert-butyl {[(1-oxo-1,3-dihydroisobenzofuran-5,6-diyl)bis(oxy)]bis(ethane-2,1-diyl)}dicarbamate (5)

A solution of compound 3 (5.00 g, 30.1 mmol) in DMF (40 mL) was charged with K₂CO; (16.6 g, 120 mmol) and stirred at rt for 5 min. The above reaction mixture was charged with compound 4 (21.1 g, 90.4 mmol) and the reaction mixture was stirred at rt for 120 h. The reaction mixture was diluted with water (300 mL) and extracted with EtOAc (3×300 mL). The combined organic layers were concentrated and the residue was purified by column chromatography (silica gel, 30-60% EtOAc in hexanes) to afford compound 5 (8.00 g, 59%) as a white gum: ¹H NMR (400 MHz, CD₃OD) δ 7.72 (s, 1H), 7.16 (s, 1H), 5.24 (s, 2H), 4.14 (t, J=5.7 Hz, 2H), 4.08 (t, J=5.7 Hz, 2H), 3.54-3.44 (m, 4H), 1.43 (s, 18H).

Preparation of di-tert-butyl ({[4,5-bis(hydroxymethyl)-1,2-phenylene]bis(oxy)}bis(ethane-2,1-diyl))dicarbamate (6)

A solution of compound 5 (5.00 g, 11.0 mmol) in THF (50 mL) was charged with lithium aluminum hydride (1 M solution in diethyl ether, 33.2 mL, 33.2 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 1 h and quenched with ice-cold water at 0° C. The reaction mixture was diluted with chloroform (300 mL) and filtered through a Celite pad, and the Celite pad was washed with chloroform (2×300 ml). The filtrate was concentrated under vacuum to afford 6 (4.50 g, 90%) as a colorless gum: ¹H NMR (400 MHz, DMSO-d₆) δ 6.99 (s, 2H), 6.90 (t, J=5.9 Hz, 2H), 4.97 (brs, 2H), 4.44 (s, 4H), 3.92 (t, J=5.6 Hz, 4H), 3.30-3.22 (m, 4H), 1.38 (s, 18H).

Preparation of S,S′-((4,5-bis(2-((tert-butoxycarbonyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate (7)

A solution of 6 (4.50 g, 9.95 mmol) in CH₂Cl₂ (100 mL) was charged with Et₃N (10.9 mL, 79.6 mmol) followed by methanesulfonyl chloride (3.00 mL, 39.8 mmol) at 0° C. and stirred at rt for 12 h. The reaction mixture was diluted with water (100 mL) and extracted with CH₂Cl₂ (3×150 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford the mesylated product (8.50 g, crude) as a yellow oil, which was directly used for the next step without further purification.

The above product (8.50 g, 9.95 mmol) in a mixture of THF (200 ml) and DMF (50 mL) was charged with KSAc (2.84 g, 24.9 mmol) and stirred at rt for 16 h. The solvent was removed and the residue was partitioned between water (50.0 mL) and CH₂Cl₂ (100 mL). The CH₂Cl₂ layer was separated and the aqueous layer was extracted with CH₂Cl₂ (2×100 mL). The combined organic layers were concentrated and the residue was purified by column chromatography (silica gel, 10% to 15% EtOAc in hexanes) to afford compound 7 (4.20 g, 74% over two steps) as a yellow solid: ¹H NMR (400 MHz, CD₃OD) S 6.91 (s, 2H), 4.10 (s, 4H), 3.99 (t, J=5.7 Hz, 4H), 3.41 (t, J=5.6 Hz, 4H), 2.31 (s, 6H), 1.43 (s, 18).

Preparation of S,S′-((4,5-bis(2-aminoethoxy)-1,2-phenylene)bis(methylene)) diethanethioate (8)

Compound 7 (5.00 g, 8.74 mmol) was dissolved in 4 N HCl in dioxane (40 mL) at rt and the solution was stirred for 2 h. After concentration, the residue was triturated with MTBE to afford the hydrochloric acid salt 8 (3.50 g, 90%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.02 (s, 2H), 4.24 (1, J=5.2 Hz, 4H), 4.13 (s, 4H), 3.39 (1, J=5.3 Hz, 4H), 2.32 (s, 6H).

Preparation of S,S′-((4,5-bis(2-((S)-2,6-bis((tert-butoxycarbonyl)amino)hexanamido)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate (10)

Compound 8 (888 mg, 2.00 mmol) and acid 9 (1.38 g, 4.00 mmol) were dissolved in DMF (20 mL) and treated with DIPEA (3.49 mL, 20.0 mmol) and HATU (1.52 g, 4.00 mmol). The reaction mixture was stirred at rt for 16 h. TLC analysis of the yellow reaction mixture showed the completion of the reaction. After the solvent was removed under reduced pressure, the residue was partitioned between CH₂Cl₂ (100 mL) and NaHCO₃ (50 mL). The organic layer was separated, washed with brine (50 mL), and dried over Na₂SO₄. The organic layer was concentrated and the residue was purified by column chromatography (silica gel, 50% to 80% EtOAc in hexanes) to afford compound 10 (1.50 g, 73%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 6.88 (s, 2H), 4.10 (s, 4H), 4.09-3.96 (m, 6H), 3.63-3.55 (m, 4H), 2.97 (t, J=6.3 Hz, 4H), 2.31 (s, 6H), 1.78-1.67 (m, 2H), 1.65-1.55 (m, 2H), 1.50-1.25 (m, 8H), 1.42 (s, 18H), 1.40 (s, 18H).

Preparation of S,S′-((4,5-bis(2-((S)-2,6-diaminohexanamido)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (11)

Compound 10 (268 mg, 0.26 mmol) was dissolved in 4 N HCl in dioxane (8.0 mL) at rt and the solution was stirred for 3 h. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized to afford 165 mg (82%) of pure compound 11 as a hygroscopic white solid: ¹H NMR (400 MHz, CD₃OD) δ 6.92 (s, 2H), 4.11 (s, 4H), 4.08 (t, J=5.3 Hz, 4H), 3.94 (t, J=4.7 Hz, 2H), 3.72-3.56 (m, 4H), 2.90 (d, J=7.2 Hz, 2H), 2.87 (d, J=7.6 Hz, 2H), 2.33 (s, 6H), 1.99-1.81 (m, 4H), 1.75-1.65 (m, 4H), 1.55-1.44 (m, 4H); ESI MS m/z 629 [M+H].⁺

2. Preparation of S,S′-(1,2-phenylenebis(methylene)) diethanethioate (13)

Preparation of of S,S′-(1,2-phenylenebis(methylene)) diethanethioate (13)

A solution of compound 12 (2.00 g, 7.50 mmol) in CH₂Cl₂ (70 ml) was charged with Et₃N (3.00 mL, 22.5 mmol) followed by AcSH (1.06 mL, 15.0 mmol). The reaction mixture was stirred at rt for 16 h. Water (50 mL) and CH₂Cl₂ (70 ml) were added to the reaction mixture. The CH₂Cl₂ layer was separated and the aqueous layer was extracted with CH₂Cl₂ (2×30 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 5% to 20% EtOAc in hexanes) to afford compound 13 (1.20 g, 63%) as a red brown oil: ¹H NMR (400 MHz, CDCl₃) δ 7.33-7.27 (m, 2H), 7.22-7.17 (m, 2H), 4.17 (s, 4H), 2.34 (s, 6H); ¹H NMR (400 MHz, CD₃OD) δ 7.32-7.25 (m, 2H), 7.20-7.16 (m, 2H), 4.18 (s, 4H), 2.32 (s, 6H); ESI MS m/z 255 [M+H].⁺

3. Preparation of S,S′-(pyrazine-2,3-diylbis(methylene)) diethanethioate (15)

A solution of compound 14 (3.00 g, 11.3 mmol) in CH₂Cl₂ (70 ml) was charged with Et₃N (3.40 mL, 24.8 mmol) followed by AcSH (1.76, 24.8 mmol) and stirred at rt for 16 h. The solvent was removed and the residue was purified by column chromatography (silica gel, 20% to 40% EtOAc in hexanes) followed by reverse phase column to afford compound 15 (800 mg, 28%) as a yellow oil: ¹H NMR (400 MHz, CDCl₃) δ 8.40 (s, 2H), 4.42 (s, 4H), 2.38 (s, 6H); ¹H NMR (400 MHz, CD₃OD) δ 8.40 (s, 2H), 4.41 (s, 4H), 2.35 (s, 6H); ESI MS m/z 257 [M+H].⁺

4. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate (23)

Preparation of Dimethyl 4-hydroxyphthalate (17)

A solution of 4-hydroxyphthalic acid 16 (25.0 g, 137 mmol) in MeOH (500 mL) was charged with 6 N HCl in i-PrOH (46.0 mL, 274 mmol) at 0° C. and refluxed for 24 h. The solvent was removed and the residue was partitioned between saturated aqueous NaHCO₃ solution (100 mL) and EtOAc (250 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×250 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford compound 17 (25.0 g, 87%) as a brown color solid: ¹H NMR (400 MHz, CDCl₃) δ 7.72 (d, J=8.5 Hz, 1H), 7.00 (d, J=2.6 Hz, 1H), 6.91 (dd, J=8.5, 2.6 Hz, 1H), 3.89 (s, 3H), 3.85 (s, 3H).

Preparation of Dimethyl 4-{2-[(tert-butoxycarbonyl)amino]ethoxy}phthalate (18)

A solution of compound 17 (25.0 g, 119 mmol) in DMF (100 mL) was charged with KCO₃ (55.5 g, 238 mmol) and stirred at rt for 5 min. The above reaction mixture was charged with compound 4 (66.1 g, 476 mmol) and the final reaction mixture was stirred at rt for 120 h. Water (300 mL) was added to the reaction mixture and extracted with EtOAc (2×300 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 20% to 40% EtOAc in hexanes) to afford compound 18 (30.0 g, 72%) as a brown solid: ¹H NMR (400 MHz, DMSO-d₆) δ 7.78 (d, J=8.4 Hz, 1H), 7.17 (d, J=2.5 Hz, 1H), 7.01 (dd, J=8.4, 2.5 Hz, 1H), 7.01 (t, J=6.0 Hz, 1H), 4.08 (t, J=5.5 Hz, 2H), 3.80 (s, 3H), 3.78 (s, 3H), 3.31 (t, J=6.4 Hz, 2H), 1.37 (s, 9H).

Preparation of Tert-butyl {2-[3,4-bis(hydroxymethyl)phenoxy]ethyl}carbamate (19)

A solution of compound 18 (30.0 g, 85.0 mmol) in THF (1000 mL) was charged with lithium aluminum hydride (9.68 g, 255 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 1 h and quenched with ice-cold water at 0° C. The reaction mixture was diluted with chloroform (300 mL) and filtered through a Celite pad, and the Celite pad was washed with chloroform (2×300 ml). The filtrate was concentrated under vacuum to afford 19 (20.0 g, 79%) as a yellow oil: ¹H NMR (400 MHz, CDCl₃) δ 7.23 (d, J=8.3 Hz, 1H), 6.89 (d, J=2.7 Hz, 1H), 6.78 (dd, J=8.3, 2.7 Hz, 1H), 5.10-5.01 (m, 1H), 4.65 (s, 2H), 4.64 (s, 2H), 3.99 (t, J=5.3 Hz, 2H), 3.49 (dd, J=10.6, 5.3 Hz, 2H), 1.44 (s, 9H).

Preparation of (4-{2-[(tert-butoxycarbonyl)amino]ethoxy}-1,2-phenylene)bis(methylene) dimethanesulfonate (21)

A solution of 19 (20.0 g, 67.3 mmol) in CH₂Cl₂ (600 mL) was charged with Et₃N (36.7 mL, 269 mmol) followed by methanesulfonyl chloride (13.0 mL, 168 mmol) at 0° C. and stirred at rt for 1 h. Water (200 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×200 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude 20 (27.0 g) as a brown oil which was directly used for the next step without further purification.

Crude 20 (27.0 g, 67.3 mmol) in a mixture of THF (250 ml) and DMF (60 mL) was charged with KSAc (19.2 g, 168 mmol) and stirred at rt for 16 h. The solvent was removed under reduced pressure and the reaction mixture was partitioned between water (100 mL) and EtOAc (250 mL).

The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×300 mL). The combined organic extracts were concentrated and the residue purified by column chromatography (silica gel, 100/to 20% EtOAc in hexanes) to afford compound 21 (17.0 g, 61% over two steps) as a yellow solid: ¹H NMR (400 MHz, CDCl₃) δ 7.21 (d, J=8.5 Hz, 1H), 6.84 (d, J=2.6 Hz, 1H), 6.72 (dd, J=8.5, 2.6 Hz, 1H), 5.05-4.93 (m, 1H), 4.11 (s, 4H), 3.97 (t, J=5.2 Hz, 2H), 3.50 (dd, J=10.8, 6.1 Hz, 2H), 2.35 (s, 3H), 2.33 (s, 3H), 1.44 (s, 9H).

*Crude product 20 was the mixture of Bis-Mesyl, Bis-Chloro and Mono-Choloro-Mono Mesyl.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (22)

Compound 21 (5.80 g, 14.0 mmol) was dissolved in 4 N HCl in dioxane (40 mL) at rt, and the solution was stirred at same temperature for 2 h. After removal of the solvent, the residue was triturated with MTBE to afford hydrochloric acid salt 22 (4.80 g, 98%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.6 Hz, 1H), 6.97 (d, J=2.8 Hz, 1H), 6.85 (dd, J=8.6, 2.8 Hz, 1H), 4.20 (dd, J=4.9, 4.3 Hz, 2H), 4.14 (s, 2H), 4.13 (s, 2H), 2.35 (t, J=4.9 Hz, 2H), 2.32 (s, 3H), 2.31 (s, 3H).

Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate (23)

A solution of amine 22 (4.80 g, 13.7 mmol) in methanol (110 mL) was charged with D-glucose (7.40 g, 41.0 mmol) and acetic acid (4.0 mL, 69.0 mmol) successively and stirred at rt for 10 min. Sodium cyanoborohydride (2.60 g, 41.0 mmol) was added to the above reaction mixture and the resulting reaction mixture was stirred at room temperature for 24 h. Additional D-glucose (3.72 g, 20.6 mmol), AcOH (1.24 mL, 20.6 mmol), and Sodium cyanoborohydride (1.30 g, 20.6 mmol) were charged and the mixture was stirred for another 24 h. Further additional D-glucose (3.72 g, 20.6 mmol), AcOH (1.24 mL, 20.6 mmol), and Sodium cyanoborohydride (1.30 g, 20.6 mmol) were charged and the mixture was stirred for another 48 h. After the solvent was removed under reduced pressure, the residue was neutralized with saturated aqueous NaHCO₃, concentrated and residue was purified by reverse-phase chromatography using a C18 Gold column to get pure 23 (3.13 g, 36%) as a white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.19 (d, J=8.4 Hz, 1H); 6.89 (d, J=2.5 Hz, 1H), 6.80 (dd, J=8.4, 2.5 Hz, 1H), 4.14 (s, 2H), 4.12 (s, 2H), 4.13-4.06 (m, 2H), 3.93-3.85 (m, 2H), 3.83-3.73 (m, 4H), 3.73-3.66 (m, 3H), 3.66-3.53 (m, 4H), 3.09-2.95 (m, 2H), 2.85-2.69 (m, 3H), 2.33 (s, 3H), 2.31 (s, 3H); ESI MS m/z 642 [M+H].⁺

5. Preparation of Compound 24

Preparation of Compound 24

A solution of amine 23 (500 mg, mmol) in pyridine (20 mL) was charged with Ac₂O (1.12 mL, 11.9 mmol) and stirred at rt for 48 h. The reaction mixture was partitioned between water (20 mL) and EtOAc (25 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×30 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 40% to 60% EtOAc in hexanes) to afford compound 24 (170 mg, 20%) as a white solid.

Alternatively:

Preparation of Compound 24

A solution of 23 (200 mg, 0.20 mmol) in CH₂Cl₂ (10 mL) was charged with Et₃N (0.30 mL, 2.00) and DMAP (25 mg, 0.02 mmol) followed by Ac₂O (0.19 mL, 2.0 mmol) and stirred at rt for 2 h. The reaction mixture was partitioned between water (20 mL) and CH₂Cl₂ (25 mL). The CH₂Cl₂ layer was separated and the aqueous layer was extracted with CH₂Cl₂ (2×30 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 40% to 60% EtOAc in hexanes) to afford compound 24 (200 mg, 94%) as a white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.19 (d, J=8.4 Hz, 1H); 6.91 (d, J=2.5 Hz, 1H), 6.79 (dd, J=8.4, 2.5 Hz, 1H), 5.42 (dd, J=6.7, 5.0 Hz, 2H), 5.37 (t, J=5.0 Hz, 2H), 5.18-5.13 (m, 2H), 5.07-5.02 (m, 2H), 4.34 (dd, J=12.6, 2.9 Hz, 2H), 4.17-4.10 (m, 6H), 3.99 (t, J=5.8 Hz, 2H), 2.93 (t, J=5.6 Hz, 2H), 2.84 (dd, J=14.1, 4.1 Hz, 2H), 2.75 (dd, J=14.1, 7.3 Hz, 2H), 2.34 (s, 3H), 2.31 (s, 3H), 2.09 (s, 6H), 2.05 (s, 6H), 2.01 (s, 6H), 2.00 (s, 6H), 1.99 (s, 6H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.20 (d, J=8.4 Hz, 1H); 6.83 (d, J=2.5 Hz, 1H), 6.77 (dd, J=8.4, 2.5 Hz, 1H), 5.29 (dd, J=6.7, 5.0 Hz, 2H), 5.24 (t, J=5.0 Hz, 2H), 5.10-5.04 (m, 2H), 5.00-4.94 (m, 2H), 4.25 (dd, J=12.6, 2.9 Hz, 2H), 4.13-4.05 (m, 6H), 3.89 (t, J=5.8 Hz, 2H), 2.95-2.84 (m, 1H), 2.80-2.62 (m, 5H); 2.35 (s, 3H), 2.33 (s, 3H), 2.05 (s, 6H), 2.02 (s, 6H), 1.98 (s, 6H), 1.97 (s, 6H), 1.96 (s, 6H); ESI MS m/z 1062 [M+H].⁺

6. Preparation of S,S′-((4-((6-aminohexyl)oxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride

Preparation of 6-bromohexan-1-amine hydrobromide (26)

A solution of compound 25 (15.0 g, 128 mmol) in hydrobromic acid 48% aq. (150 mL) was refluxed for 20 h. The reaction mixture was cooled to rt and concentrated to afford compound 26 (33 g, crude) as a yellow solid and directly used for next step without purification: ¹H NMR (400 MHz, CD₃OD) δ 3.46 (t, J=7.0 Hz, 2H), 2.94 (t, J=7.8 Hz, 2H), 1.92-1.84 (m, 2H), 1.72-1.63 (m, 2H), 1.55-1.47 (m, 2H), 1.46-1.41 (m, 2H).

Preparation of tert-butyl (6-bromohexyl)carbamate (27)

Solution of compound 26 (33 g, crude, 128 mmol) in MeOH (250 mL) was cooled to 0° C. and charged with Et₃N (35.0 mL, 256 mmol). After 5 min Boc₂O (28.0 g, 128 mmol) was added and the reaction mixture was stirred at rt for 2 h. Solvent was removed and the mixture was partitioned between EtOAc (150 mL) and NaHCO₃ solution (50 mL). The aqueous layer was separated and extracted with EtOAc (2×150 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, concentrated to afford compound 27 (35.0 g, crude) as a brown solid and directly used for next step without further purification: ¹H NMR (400 MHz, DMSO-d₆) δ 6.73 (t, J=5.3 Hz, 1H) 3.51 (t, J=6.6 Hz, 2H), 2.93-2.85 (m, 2H), 1.82-1.70 (m, 2H), 1.41-1.32 (m, 4H), 1.37 (s, 9H), 1.30-1.19 (m, 2H).

Preparation of dimethyl 4-((6-((tert-butoxycarbonyl)amino)hexyl)oxy)phthalate (28)

A solution of compound 17 (11.0 g, 52.4 mmol) in DMF (60 mL) was charged with K₂CO₃ (28.7 g, 210 mmol) and stirred at rt for 5 min. The above reaction mixture was charged with compound 27 (29.3 g, 105 mmol) and the final reaction mixture was stirred at rt for 72 h. Water (300 mL) was added to the reaction mixture and extracted with EtOAc (2×300 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 20% to 30% EtOAc in hexanes) to afford compound 28 (14.0 g, 66%, yield based on 17) as a yellow oil: ¹H NMR (400 MHz, CDCl₃) δ 7.79 (d, J=8.9 Hz, 1H); 7.04 (d, J=2.5 Hz, 1H), 6.96 (dd, J=8.9, 2.5 Hz, 1H), 4.58 (brs, 1H), 4.00 (t, J=6.4 Hz, 2H), 3.90 (s, 3H), 3.86 (s, 3H), 3.16-3.05 (m, 2H), 1.83-1.73 (m, 2H), 1.44 (s, 9H), 1.55-1.32 (m, 6H).

Preparation of tert-butyl (6-(3,4-bis(hydroxymethyl)phenoxy)hexyl)carbamate (29)

A solution of compound 28 (14.0 g, 34.2 mmol) in THF (500 mL) was charged with lithium aluminum hydride (3.90 g, 103 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 1 h then at rt for 1 h and quenched with ice-cold water at 0° C. The reaction mixture was diluted with chloroform (300 mL) and filtered through a Celite pad, and the Celite pad was washed with chloroform (2×300 ml). The filtrate was concentrated under vacuum to afford 29 (11.0 g, 90%) as a yellow solid: ¹H NMR (400 MHz, CDCl₃) δ 7.24 (d, J=8.2 Hz, 1H); 6.91 (d, J=3.0 Hz, 1H), 6.79 (dd, J=8.2, 3.0 Hz, 1H), 4.69 (s, 2H), 4.67 (s, 2H), 4.51 (brs, 1H), 3.96 (t, J=6.4 Hz, 2H), 3.74 (t, J=6.4 Hz, 2H), 3.15-3.06 (m, 2H), 1.87-1.82 (m, 2H), 1.53-1.41 (m, 4H), 1.43 (s, 9H), 1.40-1.34 (m, 2H).

Preparation of S,S′-((4-((6-((tert-butoxycarbonyl)amino)hexyl)oxy)-1,2-phenylene)bis(methylene)) diethanethioate (30)

A solution of 29 (11.0 g, 31.6 mmol) in CH₂Cl₂ (300 mL) was charged with Et₃N (17.7 mL, 126 mmol) followed by methanesulfonyl chloride (6.10 mL, 79.0 mmol) at 0° C. and stirred at rt for 1 h. The reaction mixture was diluted with water (100 mL) and extracted with CH₂Cl₂ (3×150 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford the mesylated product as (15.0 g crude) yellow oil, which was directly used for the next step without further purification.

The product (15.0 g, 31.6 mmol) in a mixture of THF (50 ml) and DMF (150 mL) was charged with KSAc (9.00 g, 79.0 mmol) and stirred at rt for 16 h. The solvent was removed and the residue was partitioned between water (50.0 mL) and EtOAc (100 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×100 mL). The combined organic layers were concentrated and the residue was purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 30 (11.0 g, 74% over two steps) as a yellow solid: ¹H NMR (400 MHz, CDCl₃) δ 7.20 (d, J=8.2 Hz, 1H); 6.83 (d, J=3.0 Hz, 1H), 6.71 (dd, J=8.2, 3.0 Hz, 1H), 4.53 (brs, 1H), 4.19 (s, 2H), 4.117 (s, 2H), 3.90 (t, J=6.4 Hz, 2H), 3.18-3.04 (m, 2H), 2.35 (s, 3H), 2.33 (s, 3H), 1.79-1.69 (m, 2H), 1.53-1.41 (m, 4H), 1.44 (s, 9H), 1.40-1.34 (m, 2H).

Preparation of compound S,S′-((4-((6-aminohexyl)oxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (31)

Compound 30 (3.60 g, 7.60 mmol) was dissolved in 4 N HCl in dioxane (30 mL) at rt and the solution was stirred for 2 h. After concentration, the residue was triturated with MTBE to afford the hydrochloric acid salt 31 (2.90 g, 94%) as an white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.18 (d, J=8.2 Hz, 1H); 6.83 (d, J=3.0 Hz, 1H), 6.73 (dd, J=8.2, 3.0 Hz, 1H), 4.129 (s, 2H), 4.123 (s, 2H), 3.95 (t, J=6.2 Hz, 2H), 2.92 (dd, J=9.4, 7.6 Hz, 2H), 2.33 (s, 3H), 2.31 (s, 3H), 1.82-1.73 (m, 2H), 1.72-1.63 (m, 2H), 1.58-1.41 (m, 4H); ¹H NMR (400 MHz, DMSO-d₆) S 7.76 (brs, 3H), 7.19 (d, J=8.2 Hz, 1H); 6.84 (d, J=3.0 Hz, 1H), 6.78 (dd, J=8.2, 3.0 Hz, 1H), 4.10 (s, 2H), 4.09 (s, 2H), 3.91 (t, J=6.6 Hz, 2H), 2.76 (t, J=7.7 Hz, 2H), 2.35 (s, 3H), 2.33 (s, 3H), 1.73-1.63 (m, 2H), 1.60-1.50 (m, 2H), 1.44-1.31 (m, 4H); ESI MS m/z 370 [M+H].⁺

7. Preparation of Compound; [ALB189175]

Preparation of Compound 32

A solution of amine 31 (2.80 g, 6.90 mmol) in methanol (35.0 mL) was charged with D-glucose (3.70 g, 20.6 mmol) and acetic acid (2.0 mL, 34.3 mmol) successively and stirred at room temperature for 10 min. Sodium cyanoborohydride (1.30 g, 20.6 mmol) was added to the above reaction mixture and the resulting reaction mixture was stirred at room temperature for 24 h. Additional D-glucose (1.86 g, 10.3 mmol), AcOH (0.61 mL, 10.3 mmol), and Sodium cyanoborohydride (649 mg, 10.3 mmol) were charged and the mixture was stirred for another 24 h. Further additional D-glucose (1.86 g, 10.3 mmol), AcOH (0.61 mL, 10.3 mmol), and Sodium cyanoborohydride (649 mg, 10.3 mmol) were charged and the mixture was stirred for another 48 h. After the solvent was removed under reduced pressure, the residue was neutralized with saturated aqueous NaHCO₃ and partially purified by reverse-phase chromatography using a C18 Gold column to get impure reductive amination product (2.50 g) which was carried forward without further purification.

800 mg of impure product (800 mg, 1.14 mmol) in CH₂Cl₂ (30 mL) was charged with Et₃N (4.0 mL, 28.5 mmol) and DMAP (139 mg, 0.11 mmol) followed by Ac₂O (2.32 mL, 22.8 mmol) and stirred at rt for 16 h. The reaction mixture was partitioned between water (20 mL) and CH₂Cl₂ (25 mL). The CH₂Cl₂ layer was separated and the aqueous layer was extracted with CH₂Cl₂ (2×30 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 32 (380 mg, 30%) as a viscous white semisolid: ¹H NMR (400 MHz, CD₃OD) δ 7.18 (d, J=8.2 Hz, 1H); 6.84 (d, J=3.0 Hz, 1H), 6.75 (dd, J=8.2, 3.0 Hz, 1H), 5.40 (dd, J=6.5, 4.3 Hz, 2H), 5.34 (t, J=4.7 Hz, 2H), 5.17-5.09 (m, 2H), 5.08-5.02 (m, 2H), 4.34 (dd, J=12.5, 2.8 Hz, 2H), 4.18-4.10 (m, 6H), 3.94 (t, J=6.3 Hz, 2H), 2.69-2.62 (m, 4H), 2.33 (s, 3H), 2.31 (s, 3H), 2.59-2.51 (m, 1H), 2.49-2.38 (m, 1H), 2.10 (s, 6H), 2.06 (s, 6H), 2.04 (s, 6H), 2.02 (s, 6H), 2.02 (s, 6H), 1.80-1.71 (m, 2H), 1.53-1.28 (m, 6H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.18 (d, J=8.4 Hz, 1H); 6.83 (d, J=2.6 Hz, 1H), 6.75 (dd, J=8.4, 2.6 Hz, 1H), 5.28 (dd, J=6.2, 4.3 Hz, 2H), 5.22 (t, J=4.8 Hz, 2H), 5.08-5.00 (m, 2H), 5.00-4.94 (m, 2H), 4.24 (dd, J=12.5, 2.8 Hz, 2H), 4.14-4.03 (m, 6H), 3.90 (t, J=6.8 Hz, 2H), 3.17 (d, J=5.2 Hz, 2H), 2.64-2.55 (m, 2H), 2.53-2.46 (m, 2H), 2.35 (s, 3H), 2.33 (s, 3H), 2.06 (s, 6H), 2.02 (s, 6H), 1.99 (s, 6H), 1.99 (s, 6H), 1.97 (s, 6H), 1.72-1.62 (m, 2H), 1.42-1.19 (m, 6H); ESI MS m/z 1118 [M+H]⁺

8. Preparation of (2S,2′S)—S,S′-(1,2-phenylenebis(methylene)) bis(2,6-diaminohexanethioate) HCl salt

Preparation of 1,2-phenylenedimethanethiol (33)

A solution of 13 (2.90 g, 11.4 mmol) in a mixture of THF (25 mL), methanol (25 mL), and water (25 mL) was charged with solid LiOH.H₂O (2.40 g, 57.0 mmol) and the reaction mixture was stirred at rt for 1 h. The above reaction mixture was charged with TCEP.HCl (1.63 g, 5.70 mmol) and stirred for another 1 h. The solvent was removed and the residue was partitioned between saturated aqueous NaHCO₃ solution (10 mL) and CH₂Cl₂ (50 mL). The CH₂Cl₂ layer was separated and the aqueous layer was extracted with CH₂Cl₂ (2×30 mL). The combined organic layers were dried over Na₂SO₄, filtered, and concentrated. The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 33 (1.80 g, 93%) as a white solid: ¹H NMR (400 MHz, CDCl₃) δ 7.30-7.24 (m, 2H), 7.23-7.19 (m, 2H), 3.86 (s, 2H), 3.85 (s, 2H), 1.84 (t, J=7.2 Hz, 2H).

Preparation (2S,2′S)—S,S′-(1,2-phenylenebis(methylene)) bis(2,6-bis((tert-butoxycarbonyl)amino)hexanethioate) (34)

Compound 33 (600 mg, 3.52 mmol) and, L-Boc-Lysine-(Boc)-OH 9 (2.68 g, 7.76 mmol) were dissolved in CH₂Cl₂ (40 mL) and treated with DMAP (22.0 mg, 0.17 mmol) and EDC.HCl (2.00 g, 10.6 mmol). The reaction mixture was stirred at rt for 16 h. TLC analysis of the yellow reaction mixture showed completion of the reaction. After the solvent was removed under reduced pressure, the residue was dissolved in CH₂Cl₂ (100 mL). The solution was quickly washed with saturated aqueous NaHCO₃ (2×25 mL) and brine (25 mL) and dried over Na₂SO₄. The organic layer was filtered, concentrated and the residue purified by column chromatography (silica gel, 40% to 50% EtOAc in hexanes) to afford compound 34 (2.00 g, 68%) as a white solid: ¹H NMR (400 MHz, CDCl₃) δ 7.30-7.24 (m, 2H), 7.21-7.15 (m, 2H), 5.23 (brs, 2H), 4.64 (brs, 2H), 4.38-4.91 (m, 2H), 4.13 (s, 2H), 4.13 (s, 2H), 3.16-3.02 (m, 4H), 1.93-1.77 (m, 2H), 1.70-1.57 (m, 2H), 1.54-1.31 (m, 8H), 1.44 (s, 36H).

Preparation of (2S,2′S)—S,S′-(1,2-phenylenebis(methylene)) bis(2,6-diaminohexanethioate)HCl salt (35)

Compound 34 (826 mg, 1.00 mmol) was dissolved in 4 N HCl in dioxane (15 mL) at rt and the solution was stirred for 1 h. After concentration, the residue was triturated with MTBE to afford the hydrochloric acid salt 31 (500 mg, 87%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.43-7.36 (m, 2H), 7.29-7.22 (m, 2H), 4.418 (s, 2H), 4.42 (s, 2H), 4.33 (dd, J=7.0, 5.9 Hz, 2H), 3.92 (t, J=8.2 Hz, 4H), 2.10-1.99 (m, 2H), 1.99-1.87 (m, 2H), 1.77-1.65 (m, 4H), 1.61-1.40 (m, 4H); ¹H NMR (400 MHz, DMSO-d₆) 8.64 (brs, 4H), 7.93 (brs, 5H), 7.49-7.42 (m, 2H), 7.30-7.24 (m, 2H), 4.33 (s, 4H), 4.29-4.21 (m, 2H), 2.72 (t, J=7.6 Hz, 4H), 1.90-1.74 (m, 4H), 1.60-1.50 (m, 4H), 1.49-1.39 (m, 2H), 1.38-1.28 (m, 2H); ESI MS m/z 427 [M+H].⁺

9. Preparation of 7,8-dimethyl-3-phenoxy-1,5-dihydrobenzo[e][1,3,2]dithiaphosphepine 3-oxide (38); [ALB176290]; SG-SJL-D-139

To a solution of compound 36 (300 mg, 1.51 mmol) and Et₃N (0.40 mL, 3.02 mmol) in toluene (6.0 mL) was added a solution of 37 (0.21 mL, 1.51 mmol) in toluene (2 mL) at 45° C. and stirred at 45° C. for 3 h. Solid was filtered and filtrate was concentered. The residue was purified by column chromatography (silica gel, 20% to 30% EtOAc in hexanes) followed by reverse phase column (C-18) to afford compound 38 (40 mg, 8.0%) as a white solid:

¹H NMR (400 MHz. CD₃OD) δ 7.46-7.36 (m, 4H), 7.31-7.25 (m, 1H), 7.15 (s, 2H), 4.41 (d, J=14.4 Hz, 1H), 4.37 (d, J=14.4 Hz, 1H), 4.18 (d, J=15.2 Hz, 1H), 4.11 (d, J=14.8 Hz, 1H), 2.26 (s, 6H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.42 (s, 2H), 7.45 (s, 2H), 7.32-7.26 (m, 1H), 7.20 (s, 2H), 4.40 (t, J=14.7 Hz, 2H), 4.26 (d, J=14.4 Hz, 1H), 4.19 (d, J=14.4 Hz, 1H), 2.26 (s, 6H); ESI MS m/z 337 [M+H].⁺

10. Preparation of tert-butyl (2-((3-oxido-3-phenoxy-1,5-dihydrobenzo[e][1,3,2]dithiaphosphepin-7-yl)oxy)ethyl)carbamate (40); [ALB176166]; SG-SJL-D-140

To a solution of compound 39 (1.20 g, 3.60 mmol) and Et₃N (0.98 mL, 7.20 mmol) in toluene (15 mL) was added a solution of 37 (0.50 mL, 3.60 mmol) in toluene (2 mL) at 45° C. and stirred at 45° C. for 3 h. Solid was filtered and filtrate was concentered. The residue was purified by column chromatography (silica gel, 20% to 30% EtOAc in hexanes) followed by reverse phase column (C-18) to afford compound 40 (72 mg, 4.0%) as a white solid:

¹H NMR (400 MHz, CD₃OD) δ 7.47-7.37 (m, 4H), 7.29-7.24 (m, 1H), 7.31 (d, J=8.4H, 1H), 6.99 (d, J=2.7 Hz, 1H), 6.92 (dd, J=8.4, 2.7 Hz, 1H); 4.42 (ddd, J=16.7, 14.9, 2.3 Hz, 2H), 4.22 (dd, J=14.9, 11.9 Hz, 1H), 4.14 (dd, J=14.9, 12.0 Hz, 1H), 4.02 (t, J=6.0 Hz, 2H), 3.42 (t, J=6.0 Hz, 2H), 1.43 (s, 9H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.47 (s, 2H), 7.46 (s, 2H), 7.36 (d, J=8.5H, 1H), 7.32-7.26 (m, 1H), 7.05 (d, J=2.7 Hz, 1H), 7.02-6.97 (m, 1H), 6.90 (dd, J=8.4, 2.7 Hz, 1H), 4.41 (t, J=14.7 Hz, 2H), 4.31 (dd, J=16.1, 14.4 Hz, 1H), 4.23 (dd, J=14.4, 12.1 Hz, 1H), 3.96 (t, J=6.1 Hz, 2H), 3.28 (t, J=6.1 Hz, 2H), 1.35 (s, 9H); ESI MS m/z 490 [M+Na]⁺.

Parent Molecules Tested

Materials and Methods

All commercial materials were used as supplied unless otherwise noted. All solvents were reagent grade or HPLC grade. Anhydrous THF, MeOH, CH₂Cl₂ were purchased from Sigma-Aldrich and used without further drying. All reactions were performed under an atmosphere of pre-purified dry Ar(g). NMR spectra were recorded on Bruker Avance-400 instrument and Solvents CDCl₃, CD₃OD and DMSO-d₆ were purchased from Aldrich or Cambridge Isotope Laboratories, unless otherwise specified. The following abbreviations were used to explain the multiplicities: s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet, and br=broad. Chemical shifts are reported in ppm relative to tetramethylsilane (TMS) as the internal standard. Microwave reactions were performed on a Biotage microwave reactor. All reactions were carried out in oven-dried glassware under argon atmosphere unless otherwise noted. Reactions were monitored by TLC carried out on 0.25 mm E. Merck silica-gel plates (60F-254) by using UV light as visualizing agent and ninhydrin solution and heat as developing agents. For polar compounds reactions are monitored by HPLC and LCMS analysis. E. Merck silica gel (60, particle size 0.040-0.063 mm) was used for flash-column chromatography.

LCMS and HPLC Method:

LCMS analyses were obtained using a Sunfire C18, 2.1×50 mm Analytical Column detected at 254 nm (unless otherwise specified) on a Shimadzu LCMS-LC-20AD. The following time program was used with a flow rate of 0.40 mL per minute.

HPLC analyses were obtained using XTerra MS C18 Column 5μ 4.6×150 mm Analytical Column detected at 220 nm (unless otherwise specified) on a Shimadzu HPLC system.

11. Preparation of di-isobutyryl Intermediate 48

Preparation of tert-butyl (2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)carbamate (46)

A solution of 21 (1.25 g, 3.00 mmol) in a mixture of THF (10 mL), methanol (10 mL), and water (10 mL) was charged with solid LiOH.H₂O (630 mg, 15.0 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (429 mg, 1.50 mmol) and stirred for another 1 h. The solvent was removed, the residue was dissolved in EtOAc (50 mL), and the solution was washed with saturated aqueous NaHCO₃ solution (10 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic layers were dried over Na₂SO₄, filtered, and concentrated to get crude bisthiol 46 (900 mg, 90%, yellow liquid) that was directly used for the next step without further purification. ¹H NMR (400 MHz, CDCl₃) δ 7.18 (d, J=8.4 Hz, 1H), 6.83 (d, J=2.6 Hz, 1H), 6.74 (dd, J=8.4, 2.5 Hz, 1H), 4.97 (brs, 1H), 4.00 (t, J=5.4 Hz, 2H), 3.82 (d, J=2.7 Hz, 2H), 3.80 (d, J=2.7 Hz, 2H), 3.56-3.48 (m, 2H), 1.87 (t, J=7.1 Hz, 1H), 1.81 (t, J=7.2 Hz, 1H), 1.44 (s, 9H); ESI MS m/z 330 [M+H]⁺.

Preparation of S,S′-((4-(2-((tert-butoxycarbonyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) (47)

To a solution of compound 46 (900 mg, 2.72 mmol) and Et₃N (2.22 mL, 16.3 mmol) in CH₂Cl₂ (20 mL) was added isobutyryl chloride (0.86 mL, 8.18 mmol) 0° C. dropwise and stirred at rt for 1 h. Water (20 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×40 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude 47 (1.40 g) as a brown oil which was directly used for the next step without further purification: ¹H NMR (400 MHz, CDCl₃) δ 7.20 (d, J=8.3 Hz, 1H), 6.83 (d, J=2.5 Hz, 1H), 6.72 (dd, J=8.2, 2.5 Hz, 1H), 4.97 (brs, 1H), 4.10 (s, 4H), 3.97 (t, J=5.2 Hz, 2H), 3.50-3.46 (m, 2H), 2.97-2.68 (m, 2H), 1.44 (s, 9H), 1.23 (d, J=3.6 Hz, 6H), 1.20 (d, J=2.9 Hz, 6H); ESI MS m/z 470 [M+H]⁺.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (48)

Compound 11 (1.40 g, crude, 2.72 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 1 h. After concentration, the residue was triturated with EtOAc to afford the hydrochloric acid salt 12 (900 mg, 82%, over two steps) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=7.9 Hz, 1H), 6.97 (d, J=2.6 Hz, 1H), 6.85 (dd, J=7.9, 2.6 Hz, 1H), 4.20 (t, J=5.4 Hz, 2H), 4.14 (s, 2H), 4.11 (s, 2H), 3.34 (t, J=5.9 Hz, 2H), 2.80-2.69 (m, 2H), 1.18 (d, J=3.3 Hz, 6H), 1.16 (d, J=2.9 Hz, 6H); ESI MS m/z 370 [M+H]⁺.

12. Preparation of di-propionyl Intermediate 50

Preparation of S,S′-((4-(2-((tert-butoxycarbonyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) dipropanethioate (13)

To a solution of compound 46 (900 mg, 2.72 mmol) and Et₃N (2.22 mL, 16.3 mmol) in CH₂Cl₂ (20 mL) was added propionyl chloride (0.71 mL, 8.18 mmol) 0° C. dropwise and stirred at rt for 1 h. Solid was filtered and filtrate was concentered. Water (20 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×40 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude 49 (1.40 g) as a brown oil which was directly used for the next step without further purification: ¹H NMR (400 MHz, CDCl₃) δ 7.21 (d, J=8.5 Hz, 1H), 6.84 (d, J=2.7 Hz, 1H), 6.71 (dd, J=8.5, 2.7 Hz, 1H), 5.02-4.89 (m, 1H), 4.11 (s, 4H), 3.97 (t, J=5.9 Hz, 2H), 3.55-3.45 (m, 2H), 2.58 (q, J=7.3 Hz, 4H), 1.44 (s, 9H), 1.19 (t, J=7.3 Hz, 6H); ESI MS m/z 442 [M+H]⁺.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) dipropanethioate hydrochloride (50)

Compound 49 (1.40 g, crude, 2.72 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 1 h. After concentration, the residue was triturated with EtOAc and isolated by filtration to afford the hydrochloric acid salt 50 (950 mg, 84%, over three steps) as an brown color solid: ¹H NMR (400 MHz. CD₃OD) δ 7.25 (d, J=8.3 Hz, 1H), 6.98 (d, J=2.5 Hz, 1H), 6.85 (dd, J=8.3, 2.5 Hz, 1H), 4.19 (t, J=5.0 Hz, 2H), 4.15 (s, 2H), 4.14 (s, 2H), 3.34 (t, J=5.9 Hz, 2H), 2.58 (qd, J=7.8, 5.9 Hz 4H), 1.15 (td, J=7.5, 2.1 Hz, 6H); ESI MS m/z 342 [M+H]⁺.

13. Preparation of bis-2-furoyl Intermediate 52

Preparation of S,S′-((4-(2-((tert-butoxycarbonyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) (51)

To a solution of compound 46 (2.15 g, 6.51 mmol) and Et₃N (3.65 mL, 26.0 mmol) in CH₂Cl₂ (20 mL) was added 2-furoyl chloride (1.61 mL, 16.3 mmol) 0° C. dropwise and stirred at rt for 1 h. Water (20 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×40 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated. Residue was purified by column chromatography (silica gel, 20% to 30% EtOAc in hexanes) to afford compound 51 (3.00 g, 89%) as a white solid: ¹H NMR (400 MHz, CDCl₃) δ 7.57-7.55 (m, 2H), 7.31 (d, J=8.4 Hz, 1H), 7.19 (ddd, J=6.4, 3.4, 0.8 Hz, 2H), 6.95 (d, J=2.5 Hz, 1H), 6.74 (dd, J=8.1, 2.5 Hz, 1H), 6.54-6.51 (m, 2H), 4.96 (brs, 1H), 4.35 (s, 4H), 3.98 (t, J=5.1 Hz, 2H), 3.53-3.46 (m, 2H), 1.43 (s, 9H); ESI MS m/z 518 [M+H]⁺.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) hydrochloride (52)

Compound 51 (3.00 g, 5.80 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 1 h. After concentration, the residue was triturated with EtOAc and isolated by filtration to afford the hydrochloric acid salt 52 (2.40 g, 96% s) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.76-7.73 (m, 2H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (td, J=3.6, 0.8 Hz, 2H), 7.06 (d, J=2.7 Hz, 1H), 6.89 (dd, J=8.1, 2.7 Hz, 1H), 6.65-6.62 (m, 2H), 4.38 (s, 2H), 4.37 (s, 2H), 4.21 (t, J=5.1 Hz, 2H), 3.34 (t, J=5.2 Hz, 2H); ESI MS m/z 418 [M+H]⁺.

14. Preparation of bis-t-butyl acetate Intermediate 54

Preparation of S,S′-((4-(2-((tert-butoxycarbonyl) amino) ethoxy)-1,2-phenylene) bis (methylene)) bis(2,2-dimethylpropanethioate) (53)

To a solution of compound 46 (620 mg, 1.88 mmol) and Et₃N (0.57 mL, 3.95 mmol) in CH₂Cl₂ (100 mL) was added pivaloyl chloride (475 mg, 3.95 mmol) 0° C. dropwise and stirred at rt for 1 h. Water (100 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×100 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford 53 (700 mg, 75%) as colorless liquid which was directly used for next step without further purification; ESI MS m/z 498 [M+H]⁺.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene) bis (methylene)) bis(2,2-dimethyl propanethioate) hydrochloride (54)

Compound 53 (700 mg, 1.40 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 2 h. After concentration, the residue was triturated with EtOAc and isolated by filtration to afford the hydrochloric acid salt 54 (480 mg, 86%) as an off-white solid: ESI MS m/z 398 [M+H].

15. Preparation of bis-3-pentyl Intermediate 56

Preparation of S,S′-(4-(2-(tert-butoxycarbonylamino)ethoxy)-1,2-phenylene)bis(methylene) bis(2-ethylbutanethioate) (55)

To a solution of compound 46 (730 mg, 2.21 mmol) and Et₃N (0.65 mL, 4.65 mmol) in CH₂Cl₂ (100 mL) was added ethyl butyryl chloride (625 mg, 4.65 mmol) 0° C. dropwise and stirred at rt for 1 h. Water (100 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×100 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford 55 (520 mg, 66%) as colorless liquid which was directly used for next step without further purification; ESI MS m/z 526 [M+H]⁺.

Preparation of S,S′-(4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)bis(2-ethylbutanethioate) hydrochloride (56)

Compound 55 (520 mg, 0.988 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 2 h. After concentration, the residue was triturated with EtOAc and isolated by filtration to afford the hydrochloric acid salt 56 (370 mg, 88%) as an off-white solid: ESI MS m/z 426 [M+H]⁺.

16. Preparation of Phthalate Intermediate 58

Preparation of tert-butyl (2-((7,12-dioxo-5, 7,12,14-tetrahydrodibenzo[c,h][1,6]dithiecin-2-yl)oxy)ethyl)carbamate (57)

A solution of 46 (200 mg, 0.61 mmol) in CH₂Cl₂ (50 mL) was charged with solid phthalic acid (287 mg, 1.52 mmol), EDC.HCl (236 mg, 1.52 mmol) and followed by the addition of DMAP (37 mg, 0.31 mmol) and the reaction mixture was stirred at room temperature for 12 h. The above reaction mixture concentrated and purified by silica-gel column chromatography to afford 57 (150 mg, 55%) as an off-white solid: ¹H NMR (CDCl₃, 400 MHz): δ 7.94 (d, J=7.4 Hz, 1H), 7.72-7.68 (m, 1H), 7.64-7.60 (m, 1H), 7.51-7.49 (m, 1H), 7.19 (d, J=8.4 Hz, 1H), 6.83-6.73 (m, 2H), 5.01-4.96 (m, 3H), 4.04 (t, J=5.0 Hz, 2H), 3.82-3.68 (m, 2H), 3.55-3.53 (m, 2H), 1.44 (s, 9H); ESI-LCMS m/z 460 (M+H)⁺.

Preparation of 9-(2-aminoethoxy)dibenzo[c,h][1,6]dithiecine-5,14(7H,12H)-dione hydrochloride (58)

A solution of 57 (150 mg, 0.326 mmol) was dissolved in 4 N HCl in dioxane (10 mL) at room temperature and the solution was stirred for 2 h. The above reaction mixture concentrated and purified by reverse-phase column chromatography and lyophilized to afford 58 (75 mg, 64%) as a hygroscopic off-white solid: ¹H NMR (DMSO-d6, 400 MHz): δ 8.02-7.84 (m, 4H), 7.80-7.74 (m, 1H), 7.57 (d, J=7.6 Hz, 1H), 7.35 (d, J=8.4 Hz, 1H) 7.05 (d, J=2.6 Hz, 1H), 6.90-6.87 (m, 1H), 4.96-4.87 (m, 1H), 4.22-4.00 (m, 5H), 3.72-3.64 (m, 1H), 3.52-3.44 (m, 1H), 3.23 (t, J=4.4 Hz, 2H); ESI MS m/z 360 [M+H]⁺.

17. Preparation of S,S′-((4-(2-(bis((2S,3R,4R)-2,3,4,5-tetrahydroxypentyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (60)

Preparation of Compound 60

A solution of amine 46 (100 mg, 0.28 mmol) in methanol (5.0 mL) was charged with D-xylose (84 mg, 0.56 mmol) and acetic acid (33 mg, 0.56 mmol) successively followed by sodium cyanoborohydride (35 mg, 0.56 mmol) and the resulting reaction mixture was stirred at 60° C. for 1 h. Additional D-xylose (105 mg, 0.70 mmol), acetic acid (41 mg, 0.70 mmol) and sodium cyanoborohydride (43 mg, 0.70 mmol) were added over 3 h. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 60 (59 mg, 34%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.8 Hz, 1H), 6.96 (d, J=2.4 Hz, 1H), 6.86 (dd, J=8.8, 2.4 Hz, 1H), 4.31 (br s, 2H), 4.15-4.13 (m, 6H), 3.75-3.34 (m, 14H), 2.33 (s, 3H), 2.31 (s, 3H); ESI (m/l) [C₂₄H₃₉NO₁₁S₂+H]⁺=582.

18. Preparation of (2R,2′R,3R,3′R,4S,4′S)-5,5′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(pentane-1,2,3,4-tetraol) hydrochloride (61)

Preparation of Compound 61

A solution of 60 (148 mg, 0.25 mmol) in MeOH/water (5.0 mL/5.0 mL) was charged with solid LiOH.H₂O (53 mg, 1.27 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (35 mg, 0.12 mmol) and stirred for 1 h. The pH value of above reaction mixture was adjusted to 2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 61 (48 mg, 38%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.87 (dd, J=8.4, 2.8 Hz, 1H), 4.38 (br s, 2H), 4.20 (br s, 2H), 3.83-3.47 (m, 18H); ESI (m/z) [C₂₀H₃₅NO₉S₂+H]⁺=498.

19. Preparation of S,S′-((4-(2-(bis((S)-2,3-dihydroxypropyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (63)

Preparation of Compound 63

A solution of amine 46 (100 mg, 0.28 mmol) in methanol (5.0 mL) was charged with D-glyceraldehyde (50 mg, 0.56 mmol) and acetic acid (33 mg, 0.56 mmol) followed by sodium cyanoborohydride (35 mg, 0.56 mmol) and the resulting reaction mixture was stirred at 60° C. for 1 h. Additional D-glyceraldehyde (25 mg, 0.28 mmol), acetic acid (16 mg, 0.28 mmol) and sodium cyanoborohydride (17 mg, 0.28 mmol) were added and the reaction mixture con stirred at 60° C. for 1 h. Additional D-glyceraldehyde (12.5 mg, 0.14 mmol), acetic acid (8 mg, 0.14 mmol) and sodium cyanoborohydride (8.5 mg, 0.14 mmol) were added and stirred at 60° C. for 1 h. Additional D-glyceraldehyde (12.5 mg, 0.14 mmol), acetic acid (8 mg, 0.14 mmol) and sodium cyanoborohydride (8.5 mg, 0.14 mmol) were added and stirred at 60° C. for 30 min. Additional D-glyceraldehyde (12.5 mg, 0.14 mmol), acetic acid (8 mg, 0.14 mmol) and sodium cyanoborohydride (8.5 mg, 0.14 mmol) were added and continued to be stirred at 60° C. for 30 min. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions were acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 63 (103 mg, 72%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.96 (d, J=2.8 Hz, 1H), 6.86 (dd, J=8.4, 2.8 Hz, 1H), 4.34 (br s, 2H), 4.15 (s, 2H), 4.13 (s, 2H), 4.02 (br s, 2H), 3.77-3.39 (m, 10H), 2.33 (s, 3H), 2.31 (s, 3H); ESI (m/z) [C₂₀H₃₁NO₇S₂+H]⁺ 462.

20. Preparation of (2S,2′S)-3,3′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(propane-1,2-diol) hydrochloride (64)

Preparation of Compound 64; SG-GHC-M-74, 93

A solution of 63 (160 mg, 0.34 mmol) in MeOH/water (3.0 mL/3.0 mL) was charged with solid LiOH.H₂O (43 mg, 1.04 mmol) and the reaction mixture was stirred at room temperature for 2 h. The reaction mixture was charged with TCEP.HCl (195 mg, 0.68 mmol) and stirred for another 1 h. The mixture was concentrated and directly purified by reverse-phase column chromatography, to afford 148 mg of 85% pure mixture. Cyclic disulfide was observed after purification. The mixture was dissolved in water (5.0 mL) and charged with TCEP.HCl (67 mg, 0.23 mmol) and stirred for another 1 h. The pH value of above reaction mixture was adjusted to 2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 64 (32 mg, 23%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.4 Hz, 1H), 6.86 (dd, J=8.4, 2.4 Hz, 1H), 4.40-4.38 (m, 2H), 4.07 (br s, 2H), 3.86-3.29 (m, 14H); ESI (m/z) [C₁₆H₂₇NO₅S₂+H]⁺ 378.

21. Preparation of S,S′-((4-(2-(bis((2S,3R)-2,3,4-trihydroxybutyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (66)

Preparation of Compound 66

A solution of amine 46 (150 mg, 0.42 mmol) in methanol (9.0 mL) was charged with D-Erythrose (100 mg, 0.84 mmol) and acetic acid (50 mg, 0.84 mmol) successively followed by sodium cyanoborohydride (52 mg, 0.84 mmol) and the resulting reaction mixture was stirred at 55° C. for 2 h. Additional D-Erythrose (75 mg, 0.63 mmol), acetic acid (37.5 mg, 0.63 mmol) and sodium cyanoborohydride (39 mg, 0.63 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-Erythrose (50 mg, 0.42 mmol), acetic acid (25 mg, 0.42 mmol) and sodium cyanoborohydride (26 mg, 0.42 mmol) were added and continued to be stirred at 55° C. for 2 h.

After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 66 (180 mg, 73%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.36 (t, J=4.8 Hz, 2H), 4.15 (s, 2H), 4.13 (s, 2H), 4.03 (br s, 2H), 3.82-3.44 (m, 12H), 2.33 (s, 3H), 2.31 (s, 3H); ESI (m/z) [C₂₂H₃₅NO₉S₂+H]⁺ 522.

22. Preparation of (2R,2′R,3S,3′S)-4,4′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(butane-1,2,3-triol) hydrochloride (67)

Preparation of Compound 67

A solution of 66 (85 mg, 0.16 mmol) in MeOH/water (3.0 mL/3.0 mL) was charged with solid LiOH.H₂O (20 mg, 0.49 mmol) and the reaction mixture was stirred at room temperature for 2 h. The above reaction mixture was charged with TCEP.HCl (91 mg, 0.32 mmol) and stirred for another 1 h. The pH value of above reaction mixture was adjusted to 2 by addition of 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 67 (14 mg, 18%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.22 (d, J=8.8 Hz, 1H), 6.97 (d, J=2.8 Hz, 1H), 6.86 (dd, J=8.8, 2.8 Hz, 1H), 4.33 (t, J=4.8 Hz, 2H), 3.98 (br s, 2H), 3.83 (s, 2H), 3.81 (s, 2H), 3.71-3.32 (m, 12H); ESI (m/z) [C₁₈H₃₁NO₇S₂+H]⁺=438.

23. Preparation of S,S′-((4-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (68)

Preparation of Compound 68

A solution of amine 9 (800 mg, 2.28 mmol) in methanol (120 mL) was charged with D-mannose (1.23 g, 6.85 mmol) and acetic acid (411 mg, 6.85 mmol) successively followed by sodium cyanoborohydride (430 mg, 6.85 mmol) and the resulting reaction mixture was stirred at 55° C. for 3 h. Additional D-mannose (820 mg, 4.53 mmol), acetic acid (274 mg, 4.53 mmol) and sodium cyanoborohydride (286 mg, 4.53 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-mannose (820 mg, 4.53 mmol), acetic acid (274 mg, 4.53 mmol) and sodium cyanoborohydride (286 mg, 4.53 mmol) were added and continued to be stirred at 55° C. for 3 h. Additional D-mannose (820 mg, 4.53 mmol), acetic acid (274 mg, 4.53 mmol) and sodium cyanoborohydride (286 mg, 4.53 mmol) were added and continued to be stirred at 55° C. for 4 h. Water (30 mL) was added and the resulting mixture was kept in fridge for 16 h. The precipitated yellow solid was collected by filtration, to afford 1.20 g of compound 11 with 90% purity as free base. The solid acidified with 1 N HCl, to make HCl salt solution and purified by reverse-phase chromatography, to afford compound 68 (791 mg, 51%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.25 (d, J=8.8 Hz, 1H), 6.99 (d, J=2.4 Hz, 1H), 6.89 (dd, J=8.8, 2.4 Hz, 1H), 4.38 (t, J=4.0 Hz, 2H), 4.15-4.14 (m, 6H), 3.86-3.47 (m, 16H), 2.33 (s, 3H), 2.31 (s, 3H); ESI (m/z) [C₂₆H₄₃NO₃S₂+H]⁺ 642.

24. Preparation of (2R,2′R,3R,3′R,4R,4′R,5R,5′R)-6,6′-((2-((1,4-dihydrobenzo[d][1,2]dithiin-6-yl)oxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (69)

Preparation of Compound 69

A solution of 68 (450 mg, 0.66 mmol) in MeOH/water (10 mL/10 mL) was charged with solid LiOH.H₂O (142 mg, 3.31 mmol) and the reaction mixture was stirred at room temperature under an argon atmosphere for 1 h. The reaction mixture was diluted with MeOH (480 mL) and stirred with air bubbled at room temperature for 8 h. The pH value of above reaction mixture was adjusted to 2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 69 (104 mg, 26%) as a gray solid: ¹H NMR (400 MHz, D₂O) δ 7.13 (d, J=8.4 Hz, 1H), 6.89 (dd, J=8.4, 2.4 Hz, 1H), 6.83 (d, J=2.4 Hz, 1H), 4.42-4.37 (m, 2H), 4.13 (br s, 2H), 4.04 (s, 2H), 4.02 (s, 2H), 3.86-3.42 (m, 16H); ESI (m/z) [C₂₂H₃₇NO₁₁S₂+H]⁺=556.

25. Preparation of, S-4-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-2-(mercaptomethyl)benzyl ethanethioate hydrochloride and S-5-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-2-(mercaptomethyl)benzyl ethanethioate hydrochloride (70a and 70b)

Preparation of Compound 70ab

A solution of 68 (2.15 g, 3.17 mmol) in water (20 mL) was charged with 1 N HCl to adjust the pH value to 2. The reaction mixture was stirred at room temperature for 48 h. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford mixture 70ab (120 mg, 6%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.25-7.22 (m, 1H), 7.00-6.98 (m, 1H), 6.91-6.85 (m, 1H), 4.39-4.38 (m, 2H), 4.24 (s, 0.9H), 4.22 (s, 1H), 4.12 (br s, 2H), 3.83-3.47 (m, 18H), 2.34 (s, 1.3H), 2.32 (s, 1.5H); ESI (n/z) [C₂₄H₄₁NO₁₂S₂+H]⁺=600.

26. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (71)

Preparation of Compound 71

A solution of amine 22 (2.80 g, 8.00 mmol) in methanol (250 mL) was charged with D-glucose (4.32 g, 24 mmol) and acetic acid (1.44 g, 24 mmol) successively followed by sodium cyanoborohydride (1.50 g, 24 mmol) and the resulting reaction mixture was stirred at 55° C. for 3 h. Additional D-glucose (2.88 g, 16 mmol), acetic acid (0.96 g, 16 mmol) and sodium cyanoborohydride (1.00 g, 16 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-glucose (1.44 g, 8.0 mmol), acetic acid (0.48 g, 8.0 mmol) and sodium cyanoborohydride (0.50 g, 8.0 mmol) were added and continued to be stirred at 55° C. for 3 h.

After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 71 (2.48 g, 46%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.25 (d, J=8.4 Hz, 1H), 6.99 (d, J=2.4 Hz, 1H), 6.89 (dd, J=8.4, 2.4 Hz, 1H), 4.38 (t, J=4.0 Hz, 2H), 4.24-4.13 (m, 6H), 3.85-3.54 (m, 16H), 2.33 (s, 3H), 2.31 (s, 3H); ESI (m/z) [C₂₆H₄₃NO₁₃S₂+H]⁺ 642.

Preparation of Compound 71

A solution of amine 22 (8.60 g, 24.5 mmol) in methanol (150 mL) was charged with D-glucose (17.8 g, 98.3 mmol) and acetic acid (5.90 mL, 98.3 mmol) successively followed by sodium cyanoborohydride (6.20 g, 98.3 mmol) and the resulting reaction mixture was heated 50° C. and stirred at 50° C. for 4 h. After the solvent was removed under reduced pressure, the residue was acidified with 6 N HCl in iPrOH and purified by reverse-phase chromatography using a C18 Gold column to get 71 (15.0 g) as a white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.46-7.39 (m, 4H), 7.31-7.25 (m, 6H), 7.14 (d, J=8.4 Hz, 1H), 6.83 (d, J=2.4 Hz, 1H), 6.67 (dd, J=8.4, 2.5 Hz, 1H), 5.45 (s, 2H), 4.21 (dd, J=10.8, 5.6 Hz, 2H), 4.10 (s, 2H), 4.08 (s, 2H), 4.07-3.99 (m, 4H), 3.97-3.91 (m, 2H), 3.90-3.87 (m, 2H), 3.72 (dd, J=9.6, 2.1 Hz, 2H), 3.57 (t, J=10.1 Hz, 2H), 3.16-3.07 (m, 2H), 3.01 (dd, J=13.6, 4.1 Hz, 2H), 2.90 (dd, J=12.9, 9.1 Hz, 2H), 2.30 (s, 3H), 2.29 (s, 3H).

LCMS and HPLC analyses showing required product 71 (Mass [M+H]⁺ 642), acetyl cleaved product (Mass [M+H]⁺ 600) and acetyl migrated product (Mass [M+H]⁺ 684); this mixture was used for the next step for acetyl cleavage.

27. Preparation of (2R,2′R,3R,3′R,4R,4′R,5S,5′S)-6,6′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (72)

Preparation of Compound 72

A solution of 71 (15.0 g, 23.5 mmol) in water (60 mL) and charged with solid LiOH.H₂O (4.90 g, 117 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (668 mg, 2.36 mmol) and stirred for another 1 h. The pH of above reaction mixture was brought to pH=2 by aqueous 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized to afford 6.00 g (44%) of pure compound 72 as a hygroscopic off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.22 (d, J=8.5 Hz, 1H), 6.99 (d, J=2.5 Hz, 1H), 6.87 (dd, J=8.5, 2.5 Hz, 1H), 4.42-4.32 (m, 2H), 4.25-4.15 (m, 2H), 3.83 (s, 2H), 3.82 (s, 2H), 3.85-3.81 (m, 2H), 3.77 (dd, J=10.8, 3.1 Hz, 2H), 3.73-3.61 (m, 7H), 3.58-3.42 (m, 4H), 3.80-3.79 (m, 1H);

¹H NMR (400 MHz, DMSO-d₆) δ 8.63-8.52 (m, 1H), 7.22 (d, J=8.5 Hz, 1H), 6.97 (d, J=2.6 Hz, 1H), 6.85 (dd, J=8.5, 2.6 Hz, 1H), 5.52 (d, J=4.6 Hz, 1H), 5.44 (d, J=5.1 Hz, 1H), 4.81 (d, J=6.6 Hz, 2H), 4.64-4.50 (m, 4H), 4.46-4.39 (m, 2H), 4.37-4.29 (m, 2H), 4.12-3.99 (m, 2H), 3.80 (d, J=3.0 Hz, 2H), 3.79 (d, J=3.0 Hz, 2H), 3.74-3.65 (m, 4H), 3.64-3.56 (m, 2H), 3.55-3.37 (m, 10H), 2.89 (t, J=7.5 Hz, 1H), 2.81 (t, J=7.1 Hz, 1H); ESI (m/z) [C₂₂H₃₉NO₁₁S₂+H]⁺ 558.

28. Preparation of (2R,2′R,3R,3′R,4R,4′R,5S,5′S)-6,6′-((2-((1,4-dihydrobenzo[d]J[1,2]dithiin-6-yl)oxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (73)

Preparation of Compound 73

A solution of 71 (1.96 g, 2.88 mmol) in MeOH/water (50 mL/50 mL) was charged with solid LiOH.H₂O (618 mg, 14.4 mmol) and the reaction mixture was stirred at room temperature under an argon atmosphere for 1 h. The above reaction mixture was diluted with MeOH (1500 mL) and stirred with air bubbled at room temperature for 8 h. The pH value of the reaction mixture was adjusted to pH=2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 73 (465 mg, 27%) as a gray solid: ¹H NMR (400 MHz, D₂O) δ 7.14 (d, J=8.4 Hz, 1H), 6.89 (dd, J=8.4, 2.8 Hz, 1H), 6.83 (d, J=2.8 Hz, 1H), 4.45-4.33 (m, 2H), 4.18 (br s, 2H), 4.05 (s, 2H), 4.02 (s, 2H), 3.77-3.50 (m, 16H); ESI (m/z) [C₂₂H₃₇NO₁₁S₂+H]⁺ 556.

29. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (74)

Preparation of Compound 74

A solution of amine 48 (4.00 g, 9.85 mmol) in methanol (400 mL) was charged with D-glucose (3.54 g, 19.7 mmol) and acetic acid (1.18 g, 19.7 mmol) successively followed by sodium cyanoborohydride (1.23 g, 19.7 mmol) and the resulting reaction mixture was stirred at 55° C. for 2 h. Additional D-glucose (1.77 g, 9.8 mmol), acetic acid (0.59 g, 9.8 mmol) and sodium cyanoborohydride (0.61 g, 9.8 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-glucose (1.77 g, 9.8 mmol), acetic acid (0.59 g, 9.8 mmol) and sodium cyanoborohydride (0.61 g, 9.8 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-glucose (0.98 g, 4.9 mmol), acetic acid (0.29 g, 4.9 mmol) and sodium cyanoborohydride (0.30 g, 4.9 mmol) were added and continued to be stirred at 55° C. for 1 h. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 74 (3.50 g, 48%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.97 (d, J=2.8 Hz, 1H), 6.89 (dd, J=8.4, 2.8 Hz, 1H), 4.37 (br s, 2H), 4.21 (br s, 2H), 4.14 (s, 2H), 4.12 (s, 2H), 3.83-3.47 (m, 16H), 2.78-2.72 (m, 2H), 1.18 (d, J=5.6 Hz, 6H), 1.16 (d, J=5.6 Hz, 6H); ESI (m/z) [C₃₀H₅₁NO₁₃S₂+H]⁺ 698.

30. Preparation of S,S′-((4-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (75)

Preparation of Compound 75

A solution of amine 48 (1.00 g, 2.46 mmol) in methanol (40 mL) was charged with D-mannose (886 mg, 4.92 mmol) and acetic acid (295 mg, 4.92 mmol) successively followed by sodium cyanoborohydride (307 mg, 4.92 mmol) and the resulting reaction mixture was stirred at 55° C. for 2 h. Additional D-mannose (433 mg, 2.46 mmol), acetic acid (147 mg, 2.46 mmol) and sodium cyanoborohydride (153 mg, 2.46 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-mannose (433 mg, 2.46 mmol), acetic acid (147 mg, 2.46 mmol) and sodium cyanoborohydride (153 mg, 2.46 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-mannose (216 mg, 1.23 mmol), acetic acid (73 mg, 1.23 mmol) and sodium cyanoborohydride (76 mg, 1.23 mmol) were added and continued to be stirred at 55° C. for 1 h. Water (10 mL) was added and the resulting precipitated yellow solid was collected by filtration, to afford 1.50 g of compound 39 with 90% purity as free base. The solid acidified with 1 N HCl, to make HCl salt solution and purified by reverse-phase chromatography, to afford compound 75 (1.19 g, 66%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.4 Hz, 1H), 6.88 (dd, J=8.4, 2.4 Hz, 1H), 4.38 (br s, 2H), 4.14-4.12 (m, 6H), 3.82-3.30 (m, 16H), 2.77-2.72 (m, 2H), 1.18 (d, J=5.6 Hz, 6H), 1.16 (d, J=5.6 Hz, 6H); ESI (m/z) [C₃₀H₅₁NO₁₃S₂+H]⁺698.

31. Preparation of (2R,2′R,3R,3′R,4R,4′R,5R,5′R)-6,6′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (76)

Preparation of Compound 76

A solution of 75 (720 mg, 1.03 mmol) in MeOH/water (10 mL/10 mL) was charged with solid LiOH.H₂O (130 mg, 3.09 mmol) and the reaction mixture was stirred at room temperature for 2 h. The above reaction mixture was charged with TCEP.HCl (591 mg, 2.06 mmol) and stirred for 1 h. The pH value of above reaction mixture was adjusted to pH=2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 76 (403 mg, 69%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.4 Hz, 1H), 6.99 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.38 (br s, 2H), 4.11 (br s, 2H), 3.83-3.45 (m, 20H); ESI (m/z) [C₂₂H₃₉NO₁₁S₂+H]⁺=558.

32. Preparation of S,S′-((4-(2-(bis((2S,3R,4S,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (77)

Preparation of Compound 77

A solution of amine 48 (1.00 g, 2.46 mmol) in methanol (150 mL) was charged with D-galactose (886 mg, 4.92 mmol) and acetic acid (295 mg, 4.92 mmol) successively followed by sodium cyanoborohydride (307 mg, 4.92 mmol) and the resulting reaction mixture was stirred at 55° C. for 2 h. Additional D-galactose (443 mg, 2.46 mmol), acetic acid (147 mg, 2.46 mmol) and sodium cyanoborohydride (153 mg, 2.46 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-galactose (443 mg, 2.46 mmol), acetic acid (147 mg, 2.46 mmol) and sodium cyanoborohydride (153 mg, 2.46 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-galactose (221 mg, 1.23 mmol), acetic acid (74 mg, 1.23 mmol) and sodium cyanoborohydride (76 mg, 1.23 mmol) were added and continued to be stirred at 55° C. for 1 h. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 77 (995 mg, 55%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.36 (br s, 2H), 4.14 (s, 2H), 4.12 (s, 2H), 3.65 (t, J=6.4 Hz, 6H), 3.58-3.40 (m, 14H), 2.77-2.72 (m, 2H), 1.18 (d, J=5.6 Hz, 6H), 1.17 (d, J=5.6 Hz, 6H); ESI (m/z) [C₃₀H₅₁NO₁₃S₂+H]⁺ 698.

33. Preparation of (2R,2′R,3S,3′S,4R,4′R,5S,5′S)-6,6′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (78)

Preparation of Compound 78

A solution of 77 (375 mg, 0.54 mmol) in MeOH/water (5.0 mL/5.0 mL) was charged with solid LiOH.H₂O (68 mg, 1.61 mmol) and the reaction mixture was stirred at room temperature for 2 h. The above reaction mixture was charged with TCEP.HCl (154 mg, 0.54 mmol) and stirred for another 1 h. The pH value of above reaction mixture was adjusted to pH=2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 78 (61 mg, 20%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.4 Hz, 1H), 6.99 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.39 (br s, 4H), 3.90-3.35 (m, 20H); ESI (m/z) [C₂₂H₃₉NO₁₁S₂+H]⁺=558.

34. Preparation of S,S′-((4-(2-(bis((2S,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (79)

Preparation of Compound 79

A solution of amine 48 (900 mg, 2.21 mmol) in methanol (150 mL) was charged with D-allose (798 mg, 4.43 mmol) and acetic acid (265 mg, 4.43 mmol) successively followed by sodium cyanoborohydride (276 mg, 4.43 mmol) and the resulting reaction mixture was stirred at 55° C. for 2 h. Additional D-allose (399 mg, 2.21 mmol), acetic acid (132 mg, 2.21 mmol) and sodium cyanoborohydride (138 mg, 2.21 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-allose (399 mg, 2.21 mmol), acetic acid (132 mg, 2.21 mmol) and sodium cyanoborohydride (138 mg, 2.21 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-allose (200 mg, 1.10 mmol), acetic acid (66 mg, 1.10 mmol) and sodium cyanoborohydride (69 mg, 1.10 mmol) were added and continued to be stirred at 55° C. for 1 h. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 79 (912 mg, 56%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.38-4.30 (m, 4H), 4.14 (s, 2H), 4.12 (s, 2H), 3.89-3.61 (m, 16H), 2.78-2.72 (m, 2H), 1.18 (d, J=5.6 Hz, 6H), 1.17 (d, J=5.6 Hz, 6H); ESI (m/z) [C₃₀H₅₁NO₁₃S₂+H]⁺ 698.

35. Preparation of (2R,2′R,3R,3′R,4S,4′S,5S,5′S)-6,6′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (80)

Preparation of Compound 80

A solution of 79 (380 mg, 0.52 mmol) in MeOH/water (5.0 mL/5.0 mL) was charged with solid LiOH.H₂O (65 mg, 1.55 mmol) and the reaction mixture was stirred at room temperature for 2 h. The above reaction mixture was charged with TCEP.HCl (148 mg, 0.52 mmol) and stirred for another 1 h. The pH value of above reaction mixture was adjusted to pH=2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 80 (180 mg, 58%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.4 Hz, 1H), 6.99 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.40 (br s, 2H), 4.31 (br s, 2H), 3.88-3.59 (m, 20H); ESI (m/z) [C₂₂H₃₉NO₁₁S₂+H]⁺558.

36. Preparation of (2R,2′R,3R,3′R,4S,4′S,5S,5′S)-6,6′-((2-((1,4-dihydrobenzo[1,2]dithiin-6-yl)oxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (81)

Preparation of Compound 81

A solution of 80 (68 mg, 0.11 mmol) in water (34 mL) was added with satd. Na₂CO₃ to adjust the pH value to pH=11. The reaction mixture was stirred under open air at room temperature for 3 h. The pH value of above reaction mixture was adjusted to pH=2 by 1 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 81 (21 mg, 32%) as an off-white solid: ¹H NMR (400 MHz, D₂O) δ 7.11 (d, J=8.8 Hz, 1H), 6.87 (dd, J=8.4, 2.8 Hz, 1H), 6.81 (d, J=2.8 Hz, 1H), 4.24 (br s, 2H), 4.07-4.01 (m, 6H), 3.81-3.57 (m, 1H), 3.29-3.01 (m, 6H); ESI (m/z) [C₂₂H₃₇NO₁₁S₂+H]⁺=556.

37. Preparation of S,S′-((4-(2-(bis((2R,3R,4R)-2,3,4,5-tetrahydroxypentyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (82)

Preparation of Compound 82

A solution of amine 48 (800 mg, 1.97 mmol) in methanol (60 mL) was charged with D-lyxose (886 mg, 5.91 mmol) and acetic acid (354 mg, 5.91 mmol) successively followed by sodium cyanoborohydride (371 mg, 5.91 mmol) and the resulting reaction mixture was stirred at 55° C. for 3 h. Additional D-lyxose (590 mg, 3.94 mmol), acetic acid (708 mg, 3.94 mmol) and sodium cyanoborohydride (246 mg, 3.94 mmol) were added and continued to be stirred at 55° C. for 2 h. Additional D-lyxose (295 mg, 1.97 mmol), acetic acid (118 mg, 1.97 mmol) and sodium cyanoborohydride (123 mg, 1.97 mmol) were added and continued to be stirred at 55° C. for 3 h. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 82 (997 mg, 75%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.8 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.37 (t, J=4.4 Hz, 2H), 4.14-4.12 (m, 6H), 3.79-3.47 (m, 14H), 2.78-2.72 (m, 2H), 1.18 (d, J=5.6 Hz, 6H), 1.17 (d, J=5.6 Hz, 6H); ESI (m/z) [C₂₈H₄₇NO₁₁S₂+H]⁺ 638.

38. Preparation of (2R,2′R,3R,3′R,4R,4′R)-5,5′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(pentane-1,2,3,4-tetraol) hydrochloride (83)

Preparation of Compound 83

A solution of 82 (850 mg, 1.26 mmol) in MeOH/water (10 mL/10 mL) was charged with solid LiOH.H₂O (158 mg, 3.78 mmol) and the reaction mixture was stirred at room temperature for 2 h. The above reaction mixture was charged with TCEP.HCl (360 mg, 1.26 mmol) and stirred for 1 h. The pH value of above reaction mixture was adjusted to pH=2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 83 (403 mg, 60%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.23 (d, J=8.4 Hz, 1H), 6.99 (d, J=2.8 Hz, 1H), 6.88 (dd, J=8.4, 2.8 Hz, 1H), 4.40 (t, J=4.0 Hz, 2H), 4.13 (br s, 2H), 3.87-3.29 (m, 18H); ESI (m/z) [C₂₀H₃₅NO₉S₂+H]⁺ 498.

39. Preparation of (2R,2′R,3R,3′R,4R,4′R)-5,5′-((2-((1,4-dihydrobenzo[d][1,2]dithiin-6-yl)oxy)ethyl)azanediyl)bis(pentane-1,2,3,4-tetraol) hydrochloride (84)

Preparation of Compound 84

A solution of 83 (218 mg, 0.41 mmol) in MeOH/water (180 mL/20 mL) was added with satd. Na₂CO₃ to adjust the pH value to pH=11. The reaction mixture was stirred under open air at room temperature for 3 h. The pH value of above reaction mixture was adjusted to pH=2 by 1 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 84 (101 mg, 46%) as an off-white solid: ¹H NMR (400 MHz, D₂O) δ 7.13 (d, J=8.8 Hz, 1H), 6.87 (dd, J=8.8, 2.8 Hz, 1H), 6.83 (d, J=2.8 Hz, 1H), 4.37 (br s, 2H), 4.07 (br s, 2H), 4.04 (s, 2H), 4.02 (s, 2H), 3.84-3.38 (m, 14H); ESI (m/z) [C₂₀H₃₃NO₉S₂+H]⁺ 496.

40. Preparation of S,S′-((4-(2-(bis((2S,3S,4R)-2,3,4,5-tetrahydroxypentyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (85)

Preparation of Compound 85

A solution of amine 48 (900 mg, 2.43 mmol) in methanol (50 mL) was charged with D-Ribose (730 mg, 4.86 mmol) and acetic acid (0.3 mL, 4.86 mmol) followed by sodium cyanoborohydride (306 mg, 4.86 mmol) and the resulting reaction mixture was stirred at room temperature for 2 h at 55° C. Additional D-Ribose (1.0 equiv), AcOH (1.0 equiv), and sodium cyanoborohydride (1.0 equiv) were charged and the mixture was stirred for 2 h at 55° C. Further additional D-Ribose (1.0 equiv), AcOH (1.0 equiv), and sodium cyanoborohydride (1.0 equiv) were charged and the mixture was stirred for 2 h at 55° C. After the solvent was removed under reduced pressure it was acidified with 4 N aq. HCl, the residue was purified by reverse-phase chromatography using a C18 Gold column to get pure 85 (900 mg, 58%) as a white solid: ¹H NMR (400 MHz, DMSO-d6) δ 7.20 (d, J=8.6 Hz, 1H), 6.85-6.78 (m, 2H), 4.65-4.45 (m, 6H), 4.30 (t, J=5.6 Hz, 2H), 4.09 (s, 2H), 4.08 (s, 2H), 4.02 (t, J=6.2 Hz, 2H), 3.69 (br s, 2H), 3.59-3.52 (m, 2H), 3.50-3.43 (m, 2H), 3.41-3.34 (m, 4H), 2.99-2.67 (m, 6H), 2.62-2.53 (m, 2H), 1.13 (s, 3H), 1.12 (s, 3H), 1.11 (s, 3H), 1.10 (s, 3H); ESI MS m/z 638 [M+H]⁺.

41. Preparation of (2R,2′R,3S,3′S,4S,4′S)-5,5′-((2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)azanediyl)bis(pentane-1,2,3,4-tetraol) hydrochloride (86) Scheme 41

Preparation of Compound 86

A solution of 85 (450 mg, 0.67 mmol) in MeOH/water (3.0 mL/3.0 mL) was charged with solid LiOH.H₂O (85 mg, 2.00 mmol) and the reaction mixture was stirred at room temperature for 2 h. The above reaction mixture was charged with TCEP.HCl (383 mg, 1.34 mmol) and stirred for another 1 h. The crude was concentrated and directly purified by reverse-phase column chromatography, to afford 120 mg of mixture. Cyclic disulfide was observed after purification. The mixture was dissolved in MeOH/water (8.0 mL/2.0 mL) and charged with TCEP.HCl (64 mg, 0.22 mmol) and stirred for another 1 h. The pH value of above reaction mixture was adjusted to pH=2 using 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized, to afford compound 86 (33 mg, 9%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.22 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.87 (dd, J=8.4, 2.8 Hz, 1H), 4.35 (t, J=4.4 Hz, 2H), 4.20 (br s, 2H), 3.83 (s, 2H), 3.82 (s, 2H), 3.77-3.47 (m, 14H); ESI (m/z) [C₂₀H₃₅NO₉S₂+H]⁺=498.

42. Preparation of S,S′-((4-(2-(bis((2R,3S,4R)-2,3,4,5-tetrahydroxypentyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (87)

Preparation of Compound 87

A solution of amine 48 (1.00 g, 2.70 mmol) in methanol (50 mL) was charged with D-arabinose (810 mg, 5.40 mmol) and acetic acid (0.32 mL, 5.40 mmol) followed by sodium cyanoborohydride (340 mg, 5.40 mmol) and the resulting reaction mixture was stirred at room temperature for 2 h at 55° C. Additional D-arabinose (405 mg, 2.70 mmol), AcOH (0.16 mL, 2.70 mmol), and sodium cyanoborohydride (170 mg, 2.70 mmol) were charged and the mixture was stirred for 2 h at 55° C. Further additional D-arabinose (405 mg, 2.70 mmol), AcOH (0.16 mL, 2.70 mmol), and sodium cyanoborohydride (170 mg, 2.70 mmol) were charged and the mixture was stirred for 2 h at 55° C. After the solvent was removed under reduced pressure it was acidified with 4 N aq. HCl, the residue was purified by reverse-phase chromatography using a C18 Gold column to get pure 87 (1.10 g, 65%) as a hygroscopic off-white solid: ¹H NMR (400 MHz, DMSO-d6) δ 8.59 (br s, 1H), 7.22 (br s, 1H), 6.96-6.75 (m, 2H), 5.23-5.04 (m, 1H), 4.93-4.78 (m, 1H), 4.66 (br s, 1H), 4.47 (br s, 2H), 4.39-4.05 (m, 9H), 4.01 (br s, 1H), 3.87-3.66 (m, 2H), 3.60 (br s, 2H), 3.54-3.35 (m, 6H), 3.24 (br s, 2H), 2.92 (br s, 1H), 2.81-2.69 (m, 2H), 2.61 (br s, 1H), 1.13 (s, 3H), 1.12 (s, 3H), 1.11 (s, 3H) 1.10 (s, 3H); ESI MS m/z 638 [M+H]⁺.

43. Preparation of (2R,2′R,3S,3′S,4R,4′R)-5,5′-((2-(3,4-bis(mercaptomethyl) phenoxy)ethyl) azanediyl)bis(pentane-1,2,3,4-tetraol) hydrochloride (88)

Preparation of Compound 88

A solution of 87 (500 mg, 0.78 mmol) in water (20 mL) and charged with solid LiOH.H₂O (100 mg, 2.35 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (446 mg, 1.56 mmol) and stirred for 1 h. The pH of above reaction mixture was brought to pH=2 by aqueous 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized to afford 88 (105 mg, 25%) as a hygroscopic off-white solid: ¹H NMR (CD₃OD, 400 MHz): δ 7.23 (d, J=8.4 Hz, 1H), 6.98 (d, J=2.8 Hz, 1H), 6.89-6.87 (m, 1H), 4.44-4.30 (m, 5H), 3.94-3.86 (m, 1H), 3.85-3.73 (m, 8H), 3.72-3.59 (m, 9H), 3.49-3.39 (m, 6H); ESI-LCMS m/z 498 (M+H)⁺.

44. Preparation of S,S′-((4-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) dipropanethioate hydrochloride (89)

Preparation of Compound 89

A solution of amine 50 (800 mg, 2.11 mmol) in methanol (50 mL) was charged with D-mannose (1.14 g, 6.35 mmol) and acetic acid (381 mg, 6.35 mmol) successively followed by sodium cyanoborohydride (398 mg, 6.35 mmol) and the resulting reaction mixture was stirred at 55° C. for 3 h. Additional D-mannose (1.14 g, 6.35 mmol), acetic acid (381 mg, 6.35 mmol) and sodium cyanoborohydride (398 mg, 6.35 mmol) were added and continued to be stirred at 55° C. for 3 h. Additional D-mannose (1.14 g, 6.35 mmol), acetic acid (381 mg, 6.35 mmol) and sodium cyanoborohydride (398 mg, 6.35 mmol) were added and continued to be stirred at 55° C. for 2 h. Water (12.5 mL) was added and the resulting mixture was kept in fridge for 4 h. The precipitated solid was collected by filtration, to afford 1.14 g of compound 89 with 95% purity as free base. The solid acidified with 1 N HCl, to make HCl salt solution and purified by reverse-phase chromatography, to afford compound 53 (495 mg, 33%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.25 (d, J=8.4 Hz, 1H), 6.99 (d, J=2.8 Hz, 1H), 6.89 (dd, J=8.4, 2.8 Hz, 1H), 4.37 (t, J=4.0 Hz, 2H), 4.16-4.14 (m, 6H), 3.86-3.47 (m, 16H), 2.63-2.56 (m, 4H), 1.18-1.13 (m, 6H); ESI (m/z) [C₂₈H₄₇NO₁₃S₂+H]⁺670.

45. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) dipropanethioate (90)

Preparation of Compound 90

A solution of amine 50 (475 mg, 1.25 mmol) in methanol (15 mL) was charged with D-glucose (724 mg, 4.00 mmol) and acetic acid (0.24 mL, 4.00 mmol) followed by sodium cyanoborohydride (252 mg, 4.00 mmol) and the resulting mixture was heated and stirred at 50° C. for 4 h. After the solvent was removed under reduced pressure, the residue was neutralized with NaHCO₃ and purified by reverse-phase chromatography using a C18 Gold column to get pure 90 (650 mg, 78%) as a white solid. ¹H NMR (400 MHz, CD₃OD) δ 7.19 (d, J=8.5 Hz, 1H), 6.89 (d, J=2.9 Hz, 1H), 6.80 (dd, J=8.5, 2.9 Hz, 1H), 4.14 (s, 2H), 4.12 (s, 2H), 4.08 (t, J=5.4 Hz, 2H), 3.93-3.86 (m, 2H), 3.81-3.74 (m, 4H), 3.73-3.67 (m, 2H), 3.66-3.58 (m, 4H), 3.12-2.94 (m, 2H), 2.85-2.72 (m, 4H), 2.58 (qd, J=8.9, 7.4 Hz, 4H), 1.15 (td, J=7.1, 4.9 Hz, 6H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.20 (d, J=8.3 Hz, 1H), 6.85 (d, J=2.1 Hz, 1H), 6.79 (dd, J=8.3, 2.1 Hz, 1H), 4.55 (brs, 2H), 4.46 (d, J=6.2 Hz, 2H), 4.35-4.32 (m, 2H), 4.29 (t, J=6.2 Hz, 2H), 4.24-4.15 (m, 2H), 4.11 (s, 2H), 4.09 (s, 2H), 4.06 (t, J=6.49 Hz, 2H), 3.72-3.65 (m, 2H), 3.62-3.53 (m, 4H), 3.52-3.44 (m, 2H), 3.44-3.33 (m, 4H), 2.96-2.83 (m, 2H), 2.69-2.53 (m, 8H), 1.07 (td, J=7.3, 4.2 Hz, 6H); ESI MS m/z 670 [C₂₈H₄₇NO₃S₂+H]⁺.

46. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) hydrochloride (91)

Preparation of Compound 91

A solution of amine 52 (1.00 g, 2.20 mmol) in methanol (50 mL) was charged with D-glucose (1.60 g, 8.83 mmol) and acetic acid (0.50 mL, 8.83 mmol) followed by sodium cyanoborohydride (556 mg, 8.83 mmol) and the resulting reaction mixture was heated and stirred at 50° C. for 4 h. Additional, D-glucose (0.40 g, 2.20 mmol) and acetic acid (0.13 mL, 2.20 mmol) successively followed by sodium cyanoborohydride (141 mg, 2.20 mmol) and the resulting reaction mixture was heated at 50° C. for another 1 h. After the solvent was removed under reduced pressure, the residue was acidified with 4 N HCl in water and purified by reverse-phase chromatography using a C18 Gold column to get 91 (550 mg, 64%) as an off-white solid.

¹H NMR (400 MHz, CD₃OD) δ 7.76-7.73 (m, 2H), 7.35 (d, J=8.3 Hz, 1H), 7.26 (ddd, J=9.0, 3.6, 0.7 Hz, 2H), 7.09 (d, J=2.9 Hz, 1H), 6.93 (dd, J=7.9, 2.9 Hz, 1H), 6.64-6.61 (m, 2H), 4.40 (t, J=4.5 Hz, 2H), 4.38 (s, 2H), 4.36 (s, 2H), 4.28-4.17 (m, 2H), 3.93-3.49 (m, 16H); ¹H NMR (400 MHz, DMSO-d₆) δ 8.71 (brs, 1H), 8.06-8.00 (m, 2H), 7.40 (ddd, J=10.1, 3.9, 0.7 Hz, 2H), 7.35 (d, J=8.6 Hz, 1H), 7.05 (d, J=2.7 Hz, 1H), 6.93 (dd, J=8.6, 2.9 Hz, 1H), 6.75 (td, J=3.6, 1.7 Hz, 2H), 4.94 (brs, 10H), 4.37 (s, 2H), 4.35 (s, 2H), 4.41-4.31 (m, 2H), 3.74-3.27 (m, 16H); ESI MS m/z 746 [C₃₂H₄₃NO₁₅S₂+H]⁺.

47. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl) amino) ethoxy)-1,2-phenylene) bis(methylene)) bis(2,2-dimethylpropanethioate) (92)

Preparation of Compound 91

A solution of amine 54 (480 mg, 1.20 mmol) in methanol (50 mL) was charged with D-glucose (1.30 g, 7.23 mmol) and acetic acid (0.43 mL, 7.23 mmol) followed by sodium cyanoborohydride (455 mg, 7.23 mmol) and the resulting mixture was stirred for 24 h at 55° C. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography using a C18 Gold column to get pure 92 (315 mg, 39%) as a white solid. ¹H NMR (DMSO-d6, 400 MHz): δ 7.20 (d, J=8.6 Hz, 1H), 6.89-6.79 (m, 2H), 4.54 (br s, 2H), 4.46 (d, J=5.6 Hz, 2H), 4.34-4.18 (m, 6H), 4.10-3.95 (m, 6H), 3.72-3.54 (m, 6H), 3.52-3.33 (m, 6H), 2.96-2.85 (m, 2H), 2.70-2.53 (m, 4H), 1.18 (s, 9H), 1.17 (s, 9H); ESI-LCMS m/z 726 (M+H)⁺.

48. Preparation of S,S′-((4-(2-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl) amino) ethoxy)-1,2-phenylene) bis(methylene)) bis(2-methylpropanethioate) hydrochloride [(93)

Preparation of Compound 93

A solution of amine 56 (370 mg, 0.86 mmol) in methanol (50 mL) was charged with D-glucose (0.94 g, 5.21 mmol) and acetic acid (0.31 mL, 5.21 mmol) followed by sodium cyanoborohydride (328 mg, 5.21 mmol) and the resulting mixture was stirred for 24 h at 55° C. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography using a C18 Gold column to get pure 93 (145 g, 24%) as a white solid ¹H NMR (CD₃OD, 400 MHz): δ 7.25 (d, J=8.6 Hz, 1H), 7.00-6.98 (m, 1H), 6.91-6.88 (m, 1H), 4.38 (br s, 2H), 4.29-4.19 (m, 2H), 4.17 (s, 2H), 4.15 (s, 2H), 3.92-3.81 (m, 3H), 3.80-3.61 (m, 9H), 3.60-3.51 (m, 4H), 2.45-2.39 (m, 2H), 1.72-1.47 (m, 8H), 0.91-0.86 (m, 12H); ESI MS m/z 755 [M+H]⁺.

Materials and Methods

All commercial materials were used as supplied unless otherwise noted. All solvents were reagent grade or HPLC grade. Anhydrous THF, MeOH, CH₂Cl₂ were purchased from Sigma-Aldrich and used without further drying. All reactions were performed under an atmosphere of pre-purified dry Ar(g). NMR spectra were recorded on Bruker Avance-400 instrument and Solvents CDCl₃, CD₃OD and DMSO-d₆ were purchased from Aldrich or Cambridge Isotope Laboratories, unless otherwise specified. The following abbreviations were used to explain the multiplicities: s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet, and br=broad. Chemical shifts are reported in ppm relative to tetramethylsilane (TMS) as the internal standard. Microwave reactions were performed on a Biotage microwave reactor. All reactions were carried out in oven-dried glassware under argon atmosphere unless otherwise noted. Reactions were monitored by TLC carried out on 0.25 mm E. Merck silica-gel plates (60F-254) by using UV light as visualizing agent and ninhydrin solution and heat as developing agents. For polar compounds reactions are monitored by HPLC and LCMS analysis. E. Merck silica gel (60, particle size 0.040-0.063 mm) was used for flash-column chromatography.

LCMS and HPLC Method:

LCMS analyses were obtained using a Sunfire C18, 2.1×50 mm Analytical Column detected at 254 nm (unless otherwise specified) on a Shimadzu LCMS-LC-20AD. The following time program was used with a flow rate of 0.40 mL per minute.

HPLC analyses were obtained using XTerra MS C18 Column 5μ 4.6×150 mm Analytical Column detected at 220 nm (unless otherwise specified) on a Shimadzu HPLC system.

49. Preparation of S,S′-((6-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)naphthalene-2,3-diyl)bis(methylene)) diethanethioate hydrochloride (12){2199-01}: ALB194811

Preparation of Dimethyl 4-hydroxyphthalate (17)

A solution of 4-hydroxyphthalic acid 16 (25.0 g, 137 mmol) in MeOH (500 mL) was charged with 6 N HCl in i-PrOH (46.0 mL, 274 mmol) at 0° C. and refluxed for 24 h. The solvent was removed and the residue was partitioned between saturated aqueous NaHCO₃ solution (100 mL) and EtOAc (250 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×250 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford compound 17 (26.1 g, 91%) as a brown solid: ¹H NMR (400 MHz, CDCl₃) δ 7.72 (d, J=8.5 Hz, 1H), 7.00 (d, J=2.6 Hz, 1H), 6.91 (dd, J=8.5, 2.6 Hz, 1H), 3.89 (s, 3H), 3.85 (s, 3H).

Preparation of tert-butyl (2-bromoethyl)carbamate (4)

A solution of compound 2-bromoethylamine (75.0 g, 366 m mol) and Et₃N (100 mL, 732 mol) in MeOH (700 mL) was charged with Boc₂O (80.0 g, 366 mol) at 0° C. The reaction mixture was stirred at room temperature for 2 h. Water (500 mL) was added and extracted with CH₂Cl₂ (2×500 mL). The organic layer was concentrated to afford compound 4 (78.0 g, 92%) as a colorless oil: ¹H NMR (400 MHz, DMSO-d₆) δ 7.08 (br s, 1H), 3.42 (d, J=6.8 Hz, 2H), 3.29 (d, J=6.8 Hz, 2H), 1.39 (s, 9H).

Preparation of Dimethyl 4-{2-[(tert-butoxycarbonyl)amino]ethoxy}phthalate (18)

A solution of compound 17 (26.1 g, 124 mmol) in DMF (100 mL) was charged with Cs₂CO₃ (81.0 g, 248 mmol) and stirred at rt for 5 min. The above reaction mixture was charged with compound 4 (57.8 g, 248 mmol) and the final reaction mixture was stirred at rt for 48 h. Water (300 mL) was added to the reaction mixture and extracted with EtOAc (2×300 mL). The combined organic extracts were concentrated and the residue was purified by column chromatography (silica gel, 20% to 40% EtOAc in hexanes) to afford compound 18 (38.0 g, 87%) as a yellow solid: ¹H NMR (400 MHz, DMSO-d₆) δ 7.78 (d, J=8.4 Hz, 1H), 7.17 (d, J=2.5 Hz, 1H), 7.01 (dd, J=8.4, 2.5 Hz, 1H), 7.01 (t, J=6.0 Hz, 1H), 4.08 (t, J=5.5 Hz, 2H), 3.80 (s, 3H), 3.78 (s, 3H), 3.31 (t, J=6.4 Hz, 2H), 1.37 (s, 9H).

Preparation of Tert-butyl {2-[3,4-bis(hydroxymethyl)phenoxy]ethyl}carbamate (19)

A solution of compound 18 (38.0 g, 108 mmol) in THF (1000 mL) was charged with lithium aluminum hydride (12.3 g, 323 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 1 h and quenched with ice-cold water at 0° C. The reaction mixture was diluted with chloroform (300 mL) and filtered through a Celite pad, and the Celite pad was washed with chloroform (2×300 ml). The filtrate was concentrated under vacuum to afford 19 (28.0 g, 94%) as a yellow oil: ¹H NMR (400 MHz, CDCl₃) δ 7.23 (d, J=8.3 Hz, 1H), 6.89 (d, J=2.7 Hz, 1H), 6.78 (dd, J=8.3, 2.7 Hz, 1H), 5.10-5.01 (m, 1H), 4.65 (s, 2H), 4.64 (s, 2H), 3.99 (t, J=5.3 Hz, 2H), 3.49 (dd, J=10.6, 5.3 Hz, 2H), 1.44 (s, 9H).

Preparation of tert-butyl (2-(3,4-diformylphenoxy)ethyl)carbamate (94)

To a solution of 19 (3.00 g, 10.0 mmol) in CH₂Cl₂ (60.0 mL) was added Dess-Martin Periodane (12.7 g, 30.0 mmol) at room temperature and reaction mixture was stirred at the room temperature for 4 h. 1 N NaOH (aqueous) was added and extracted with CH₂Cl₂ (3×100 mL). The organic layers were combined, dried over Na₂SO₄, filtered, and concentrated to afford aldehyde 94 (2.80 g, crude) as a light yellow liquid. 2.00 g of crude product was purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 94 (1.55 g) as a yellow oil: ¹H NMR (400 MHz, CDCl₃) δ 10.64 (s, 1H), 10.33 (s, 1H), 7.93 (d, J=8.6 Hz, 1H), 7.45 (d, J=2.4 Hz, 1H), 7.22 (dd, J=8.6, 2.4 Hz, 1H), 4.98 (brs, 1H), 4.17 (t, J=5.5 Hz, 2H), 3.62-3.55 (s, 2H), 1.45 (s, 9H).

Preparation of diethyl 6-(2-((tert-butoxycarbonyl)amino)ethoxy)naphthalene-2,3-dicarboxylate (95)

To a solution of Diethyl Maleate (1.16 g, 6.80 mmol) in CH₂Cl₂ (15.0 mL) was added PEt₃ (1 M solution in THF, 7.35 mL, 7.35 mmol) at 0° C. and reaction mixture was stirred at the room temperature for 30 min. Solution of 94 (1.55 g, 5.25 mmol) in CH₂Cl₂ (15.0 mL) was added added to the above reaction mixture at 0° C. and stirred at 0° C. for 30 min. To the final reaction mixture DBU (0.79 mg, 0.52 mmol) in CH₂Cl₂ (2.0 mL) was added at 0° C. and reaction mixture was stirred at room temperature for 16 h. 10 mL water was added to the reaction mixture and extracted with CH₂Cl₂ (3×20 mL). The organic layers were combined, dried over Na₂SO₄, filtered, and concentrated and purified by column chromatography (silica gel, 20% to 30% EtOAc in hexanes) to afford compound 95 (1.80 g, 80%) as a colorless oil: ¹H NMR (400 MHz, CDCl₃) δ 8.21 (s, 1H), 8.04 (s, 1H), 7.81 (d, J=8.4 Hz, 1H), 7.25 (dd, J=8.4, 2.4 Hz, 1H), 7.18-7.14 (m, 1H), 5.06 (brs, 1H), 4.40 (qd, J=7.2, 5.6 Hz, 4H), 4.14 (t, J=4.8 Hz, 2H), 3.65-3.53 (s, 2H), 1.45 (s, 9H), 1.40 (td, J=7.3, 1.3 Hz, 6H).

Preparation of tert-butyl (2-((6, 7-bis(hydroxymethyl)naphthalen-2-yl)oxy)ethyl)carbamate (96)

A solution of compound 95 (1.80 g, 4.27 mmol) in THF (100 mL) was charged with lithium aluminum hydride (601 mg, 15.8 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 1 h and quenched with ice-cold water at 0° C. The reaction mixture was diluted with chloroform (100 mL) and filtered through a Celite pad, and the Celite pad was washed with chloroform (2×100 ml). The filtrate was concentrated under vacuum to afford 96 (1.29 g, 87%) as a yellow oil: ¹H NMR (400 MHz, CDCl₃) S 7.72 (s, 1H), 7.71 (d, J=8.5 Hz, 1H), 7.68 (s, 1H), 7.14 (dd, J=8.5, 2.3 Hz, 1H), 7.09 (d, J=2.3 Hz, 1H), 5.04 (brs, 1H), 4.86 (s, 4H), 4.10 (t, J=5.3 Hz, 2H), 3.61-3.54 (s, 2H), 3.11 (brs, 1H), 3.02 (brs, 1H), 1.45 (s, 9H).

Preparation of S,S′-((6-(2-((tert-butoxycarbonyl)amino)ethoxy)naphthalene-2,3-diyl)bis(methylene)) diethanethioate (97)

A solution of 96 (1.29 g, 3.71 mmol) in CH₂Cl₂ (50.0 mL) was charged with Et₃N (2.00 mL, 14.8 mmol) followed by methanesulfonyl chloride (0.71 mL, 9.25 mmol) at 0° C. and stirred at rt for 1 h. Water (20.0 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×30.0 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude mesylate of 96 (2.50 g) as a brown oil which was directly used for the next step without further purification.

Crude mesylate of 96 (2.50 g) in a mixture of THF (25.0 ml) and DMF (25.0 mL) was charged with KSAc (1.00 g, 9.25 mmol) and stirred at rt for 16 h. The solvent was removed under reduced pressure and the reaction mixture was partitioned between water (50 mL) and EtOAc (100 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic extracts were concentrated and the residue purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 97 (1.35 g, 79% over two steps) as a yellow liquid: ¹H NMR (400 MHz, CDCl₃) δ 7.71 (s, 1H), 7.68 (s, 1H), 7.65 (d, J=8.9 Hz, 1H), 7.09 (dd, J=8.9, 2.6 Hz, 1H), 7.03 (d, J=2.6 Hz, 1H), 5.02 (brs, 1H), 4.29 (s, 4H), 4.10 (t, J=5.2 Hz, 2H), 3.61-3.54 (s, 2H), 2.36 (s, 3H), 2.35 (s, 3H), 1.45 (s, 9H).

Preparation of S,S′-((6-(2-aminoethoxy)naphthalene-2,3-diyl)bis(methylene)) diethanethioate hydrochloride (98)

Compound 97 (1.35 g, 2.91 mmol) was dissolved in 4 N HCl in dioxane (15 mL) at room temperature, and the solution was stirred at same temperature for 1 h. After removal of the solvent, the residue was triturated with EtOAc to afford hydrochloric acid salt 98 (1.10 g, 95%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.74 (s, 2H), 7.72 (d, J=8.9 Hz, 1H), 7.24 (d, J=2.6 Hz, 1H), 7.20 (dd, J=8.9, 2.6 Hz, 1H), 4.34 (t, J=5.2 Hz, 2H), 4.32 (s, 2H), 4.31 (s, 2H), 3.42 (t, J=5.2 Hz, 2H), 2.348 (s, 3H), 2.341 (s, 3H).

Preparation of S,S′-((6-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)naphthalene-2,3-diyl)bis(methylene)) diethanethioate hydrochloride (99)

A solution of amine 98 (1.10 g, 2.75 mmol) in methanol (35 mL) was charged with D-mannose (2.00 g, 11.0 mmol) and acetic acid (0.66 mL, 11.0 mmol) successively followed by Sodium cyanoborohydride (700 mg, 11.0 mmol) and the resulting reaction mixture was heated 55° C. and stirred at 55° C. for 2 h. Additional, D-mannose (498 mg, 2.75 mmol) and acetic acid (0.17 mL, 2.75 mmol) followed by sodium cyanoborohydride (1.0 equiv) and the resulting reaction mixture was heated stirred at 50° C. for another 1 h. Further additional, D-mannose (1.0 equiv) and acetic acid (1.0 equiv) successively followed by sodium cyanoborohydride (173 mg, 2.75 mmol) and the resulting reaction mixture was heated stirred at 55° C. for another 2 h. Reaction mixture was cooled to rt and water was added; solid precipitation came out which was filtered through filter paper and washed with water/methanol to get free base of 12 (1.25 g, 66%) as a off white solid. 1.00 g of free base 99 was then acidified with 4 N HCl in water to make HCL salt and was purified by reverse phase column (twice) to get 135 mg (13%) of HCl salt 99 as an off-white solid.

¹H NMR (400 MHz, CD₃OD) δ 7.75 (s, 2H), 7.71 (d, J=8.6 Hz, 1H), 7.27 (d, J=2.5 Hz, 1H), 7.23 (dd, J=8.6, 2.5 Hz, 1H), 4.57-4.49 (m, 2H), 4.327 (s, 2H), 4.322 (s, 2H), 4.21-4.10 (m, 2H), 4.01-3.58 (m, 14H), 3.58-3.46 (m, 2H), 2.349 (s, 3H), 2.345 (s, 3H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.80 (s, 1H), 7.78 (d, J=8.8 Hz, 1H), 7.76 (s, 1H), 7.32 (d, J=2.4 Hz, 1H), 7.23 (dd, J=8.8, 2.4 Hz, 1H), 5.68 (d, J=6.5 Hz, 1H), 5.47 (d, J=6.5 Hz, 1H), 4.70 (brs, 1H), 4.63-4.34 (m, 6H), 4.29 (s, 4H), 4.07-3.88 (m, 2H), 3.82-3.74 (m, 2H), 3.69-3.18 (m, 17H), 2.38 (s, 3H), 2.37 (s, 3H); ESI MS m/z 692 [C₃₀H₄₅NO₁₃S₂+H]⁺.

50. Preparation of (2R,2′R,3R,3′R,4R,4′R,5R,5′R)-6,6′-((2-((6, 7-bis(mercaptomethyl)naphthalen-2-yl)oxy)ethyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (100)

A solution of 99 (500 mg, 0.68 mmol) in water (20 mL) and charged with solid LiOH.H₂O (143 mg, 3.40 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (39.0 mg, 0.13 mmol) and stirred for another 1 h. The pH of above reaction mixture was brought to 2 by aqueous 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column (several times) chromatography and lyophilized to afford 30 mg (7.0%) of pure compound 100 as a hygroscopic off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.71 (s, 2H), 7.70 (d, J=8.8 Hz, 1H), 7.27 (d, J=2.4 Hz, 1H), 7.20 (dd, J=8.8, 2.4 Hz, 1H), 4.47-4.41 (m, 2H), 4.10-4.00 (m, 2H), 4.04 (s, 2H), 4.03 (s, 2H), 3.83-3.76 (m, 5H), 3.75-3.60 (m, 9H), 3.41-3.28 (m, 2H); ¹H NMR (400 MHz, DMSO-d₆) δ 7.77 (s, 1H), 7.76 (d, J=7.8 Hz, 1H), 7.75 (s, 1H), 7.32 (d, J=2.4 Hz, 1H), 7.17 (dd, J=7.8, 2.4 Hz, 1H), 7.27 (brs, 1H), 4.84-4.12 (m, 1 OH), 4.00 (dd, J=7.0, 5.0 Hz, 4H), 3.66-3.35 (m, 12H), 2.97 (td, J=7.4, 2.6 Hz, 2H); ESI MS m/z 608 [C₂₆H₄₁NO₁₁S₂+H].

51. Preparation of S,S′-((4-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) hydrochloride (102)

Preparation of (4-{2-[(tert-butoxycarbonyl)amino]ethoxy}-1,2-phenylene)bis(methylene) dimethanesulfonate (21)

A solution of 19 (30.0 g, 101 mmol) in CH₂Cl₂ (600 mL) was charged with Et₃N (55.0 mL, 404 mmol) followed by methanesulfonyl chloride (19.5 mL, 252 mmol) at 0° C. and stirred at rt for 1 h. Water (200 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×200 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude 101 (40.0 g) as a brown oil which was directly used for the next step without further purification.

Crude 101 (40.0 g) in a mixture of THF (250 ml) and DMF (50 mL) was charged with KSAc (28.8 g, 252 mmol) and stirred at rt for 16 h. The solvent was removed under reduced pressure and the reaction mixture was partitioned between water (100 mL) and EtOAc (250 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×300 mL). The combined organic extracts were concentrated and the residue purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 21 (25.0 g, 49% over two steps) as a yellow solid: ¹H NMR (400 MHz, CDCl₃) δ 7.21 (d, J=8.5 Hz, 1H), 6.84 (d, J=2.6 Hz, 1H), 6.72 (dd, J=8.5, 2.6 Hz, 1H), 5.05-4.93 (m, 1H), 4.11 (s, 4H), 3.97 (t, J=5.2 Hz, 2H), 3.50 (dd, J=10.8, 6.1 Hz, 2H), 2.35 (s, 3H), 2.33 (s, 3H), 1.44 (s, 9H).

Comments: Crude product 101 was the mixture of Bis-mesyl, Bis-chloro and Mono-choloro-Mono mesyl.

Preparation of (2-(3,4-bis(mercaptomethyl)phenoxy)ethyl)carbamate (46)

A solution of 21 (3.00 g, 7.26 mmol) in a mixture of THF (20 mL), methanol (20 mL), and water (20 mL) was charged with solid LiOH.H₂O (1.52 g, 36.3 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (1.03 g, 3.63 mmol) and stirred for another 1 h. The solvent was removed, the residue was dissolved in EtOAc (50 mL), and the solution was washed with saturated aqueous NaHCO₃ solution (10 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic layers were dried over Na₂SO₄, filtered, and concentrated to get crude bisthiol 46 (21.5 g, 90%, yellow liquid) directly used for the next step without further purification. ¹H NMR (400 MHz, CDCl₃) δ 7.18 (d, J=8.4 Hz, 1H), 6.83 (d, J=2.6 Hz, 1H), 6.74 (dd, J=8.4, 2.5 Hz, 1H), 4.97 (brs, 1H), 4.00 (t, J=5.4 Hz, 2H), 3.82 (d, J=2.7 Hz, 2H), 3.80 (d, J=2.7 Hz, 2H), 3.56-3.48 (m, 2H), 1.87 (t, J=7.1 Hz, 1H), 1.81 (t, J=7.2 Hz, 1H), 1.44 (s, 9H); ESI MS m/z 330 [M+H].

Preparation of S,S′-((4-(2-((tert-butoxycarbonyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) (51)

To a solution of compound 46 (2.15 g, 6.51 mmol) and Et₃N (3.65 mL, 26.0 mmol) in CH₂Cl₂ (20 mL) was added 2-furoyl chloride (1.61 mL, 16.3 mmol) 0° C. dropwise and stirred at rt for 1 h. Solid was filtered and filtrate was concentered. Water (20 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×40 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated. Residue was purified by column chromatography (silica gel, 20% to 30% EtOAc in hexanes) to afford compound 51 (3.00 g, 89%) as a white solid.

¹H NMR (400 MHz, CDCl₃) δ 7.57-7.55 (m, 2H), 7.31 (d, J=8.4 Hz, 1H), 7.19 (ddd, J=6.4, 3.4, 0.8 Hz, 2H), 6.95 (d, J=2.5 Hz, 1H), 6.74 (dd, J=8.1, 2.5 Hz, 1H), 6.54-6.51 (m, 2H), 4.96 (brs, 1H), 4.35 (s, 4H), 3.98 (t, J=5.1 Hz, 2H), 3.53-3.46 (m, 2H), 1.43 (s, 9H); ESI MS m/z 518 [M+H]⁺.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) hydrochloride (52)

Compound 51 (3.00 g, 5.80 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 1 h. After concentration, the residue was triturated with EtOAc to afford the hydrochloric acid salt 52 (2.40 g, 96%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.76-7.73 (m, 2H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (td, J=3.6, 0.8 Hz, 2H), 7.06 (d, J=2.7 Hz, 1H), 6.89 (dd, J=8.1, 2.7 Hz, 1H), 6.65-6.62 (m, 2H), 4.38 (s, 2H), 4.37 (s, 2H), 4.21 (t, J=5.1 Hz, 2H), 3.34 (t, J=5.2 Hz, 2H); ESI MS m/z 418 [M+H]⁺.

Preparation of S,S′-((4-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(furan-2-carbothioate) hydrochloride (102)

A solution of amine 52 (1.00 g, 2.20 mmol) in methanol (40 mL) was charged with D-mannose (1.60 g, 8.80 mmol) and acetic acid (0.50 mL, 8.80 mmol) successively followed by sodium cyanoborohydride (556 mg, 8.80 mmol) and the resulting reaction mixture was heated 50° C. and stirred at 50° C. for 6 h. Additional, D-mannose (1.0 equiv) and acetic acid (1.0 equiv) successively followed by sodium cyanoborohydride (1.0 equiv) and the resulting reaction mixture was heated stirred at 50° C. for another 1 h. Further additional, D-mannose (1.0 equiv) and acetic acid (1.0 equiv) successively followed by sodium cyanoborohydride (1.0 equiv) and the resulting reaction mixture was heated stirred at 50° C. for another 1 h. Reaction mixture was cooled to rt and water was added; after solvent was removed under reduced pressure, more water was added then solid precipitation came out which was filtered through filter paper and washed with water/methanol to get free base of the boron complex of 102 (1.10 g, 67%). 600 mg of free base of the born complex 102 was then acidified with 4 N HCl in water to make HCL salt and lyophilized to get 102 (620 mg,) as an off-white solid.

¹H NMR (400 MHz, CD₃OD) δ 7.76-7.74 (m, 2H), 7.34 (d, J=8.6 Hz, 1H), 7.26 (ddd, J=8.9, 3.5, 0.7 Hz, 2H), 7.10 (d, J=2.6 Hz, 1H), 6.93 (dd, J=8.8, 2.9 Hz, 1H), 6.63 (td, J=3.8, 1.6 Hz, 2H), 4.42-4.36 (m, 2H), 4.38 (s, 2H), 4.36 (s, 2H), 4.19-4.07 (m, 2H), 3.90-3.61 (m, 14H), 3.53-3.42 (m, 2H); ¹H NMR (400 MHz, DMSO-d₆) δ 8.04-8.00 (m, 2H), 7.40 (dd, J=9.8, 3.8, 0.7 Hz, 2H), 7.35 (d, J=9.0 Hz, 1H), 7.06-7.01 (m, 1H), 6.96-6.98 (m, 1H), 6.76 (td, J=4.1, 1.7 Hz, 2H), 4.37 (s, 2H), 4.35 (s, 2H), 4.34-3.87 (m, 15H), 3.79-3.17 (m, 16H); ESI MS m/z 746 [C₃₂H₄₃NO₁₅S₂+H]⁺.

52. Preparation of S,S′-((4-(2-(bis((2S,3R,4R)-2,3,4,5-tetrahydroxypentyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (103)

Preparation of S,S′-((4-(2-((tert-butoxycarbonyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) (47)

To a solution of compound 46 (900 mg, 2.72 mmol) and Et₃N (2.22 mL, 16.3 mmol) in CH₂Cl₂ (20 mL) was added isobutyryl chloride (0.86 mL, 8.18 mmol) 0° C. dropwise and stirred at rt for 1 h. Water (20 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×40 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude 47 (1.40 g) as a brown oil which was directly used for the next step without further purification.

¹H NMR (400 MHz, CDCl₃) δ 7.20 (d, J=8.3 Hz, 1H), 6.83 (d, J=2.5 Hz, 1H), 6.72 (dd, J=8.2, 2.5 Hz, 1H), 4.97 (brs, 1H), 4.10 (s, 4H), 3.97 (t, J=5.2 Hz, 2H), 3.50-3.46 (m, 2H), 2.97-2.68 (m, 2H), 1.44 (s, 9H), 1.23 (d, J=3.6 Hz, 6H), 1.20 (d, J=2.9 Hz, 6H); ESI MS m/z 470 [M+H]⁺.

Preparation of S,S′-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (48)

Compound 47 (1.40 g, crude, 2.72 mmol) was dissolved in 4 N HCl in dioxane (20 mL) at room temperature and the solution was stirred for 1 h. After concentration, the residue was triturated with EtOAc to afford the hydrochloric acid salt 48 (900 mg, 82%, over two steps) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=7.9 Hz, 1H), 6.97 (d, J=2.6 Hz, 1H), 6.85 (dd, J=7.9, 2.6 Hz, 1H), 4.20 (t, J=5.4 Hz, 2H), 4.14 (s, 2H), 4.11 (s, 2H), 3.34 (t, J=5.9 Hz, 2H), 2.80-2.69 (m, 2H), 1.18 (d, J=3.3 Hz, 6H), 1.16 (d, J=2.9 Hz, 6H); ESI MS m/z 370 [M+H]⁺.

Preparation of S,S′-((4-(2-(bis((2S,3R,4R)-2,3,4,5-tetrahydroxypentyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) bis(2-methylpropanethioate) hydrochloride (103)

A solution of amine 48 (500 mg, 1.35 mmol) in methanol (60 mL) was charged with D-Xylose (608 mg, 4.05 mmol) and acetic acid (0.25 mL, 4.05 mmol) successively followed by sodium cyanoborohydride (255 mg, 4.05 mmol) and the resulting reaction mixture was stirred for 3 h at 55° C. Additional D-Xylose (405 mg, 2.70 mmol), sodium cyanoborohydride (150 mg, 2.70 mmol) and acetic acid (0.16 mL, 2.70 mmol) were charged and the mixture was stirred for 2 h at 55° C. Further D-Xylose (202 mg, 1.35 mmol), sodium cyanoborohydride (75 mg, 1.35 mmol) and acetic acid (0.08 mL, 1.35 mmol) were charged and the mixture was stirred for 1 h at 55° C. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase chromatography. The pure fractions was acidified with 1 N HCl until pH=3 and lyophilized, to afford compound 103 (668 mg, 80%) as an off-white solid: ¹H NMR (400 MHz, CD₃OD) δ 7.24 (d, J=8.4 Hz, 1H), 6.97 (d, J=2.4 Hz, 1H), 6.86 (dd, J=8.4, 2.4 Hz, 1H), 4.31 (br s, 2H), 4.14-4.12 (m, 6H), 3.77-3.47 (m, 14H), 2.78-2.72 (m, 2H), 1.18 (d, J=5.6 Hz, 1H), 1.17 (d, J=5.6 Hz, 1H); ESI (m/z) [C₂₈H₄₇NO₁S₂+H]⁺ 638.

53. Preparation of S,S′-((4-(3-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl) amino) propyl)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (109)

Preparation of tert-butyl (3-(1-oxo-1,3-dihydroisobenzofuran-5-yl)propyl)carbamate; (103)

To a solution of compound 104 (3.00 g, 19.10 mmol) in anhydrous THF (300 mL) was added 9-BBN (0.5 M in THF, 96 mL, 47.70 mmol) under argon. After the reaction mixture was stirred for 2 h at room temperature, compound 103 (3.25 g, 15.28 mmol), Pd(PPh₃)₂Cl₂ (670 mg, 0.95 mmol), and 2 N aq Na₂CO₃ (75 mL) were added at room temperature. The resulting mixture was stirred for additional 1 h. After solvent removed; the residue was partitioned between EtOAc (200 mL) and water (200 mL). The aqueous layer was separated and extracted with EtOAc (2×200 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄ and concentrated under vacuum. The crude product was purified by silica-gel column chromatography to get 105 (1.50 g, 34%); ¹H NMR (CDCl₃, 400 MHz): δ 7.23-7.18 (m, 1H), 6.83 (s, 1H), 6.74-6.69 (m, 1H), 5.08 (br s, 1H), 4.22 (s, 4H), 3.95 (br s, 2H), 3.47 (br s, 2H), 1.43 (s, 9H); ESI-LCMS m/z 292 (M+H)⁺.

Preparation of tert-butyl (3-(3,4-bis(hydroxymethyl)phenyl)propyl)carbamate (106)

A solution of compound 105 (1.50 g, 5.15 mmol) in THF (150 mL) was charged with lithium aluminum hydride (525 mg, 15.46 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 1 h and quenched with ice-cold water at 0° C. The reaction mixture was diluted with chloroform (300 mL) and filtered through a Celite pad, and the Celite pad was washed with chloroform (2×300 ml). The filtrate was concentrated under vacuum to afford 106 (1.30 g, 86%) as a yellow oil which was directly used for next step without further purification.

Preparation of S,S′-((4-(3-((tert-butoxycarbonyl) amino) propyl)-1,2-phenylene) bis (methylene)) diethanethioate (107)

A solution of 106 (1.30 g, 4.40 mmol) in CH₂Cl₂ (100 mL) was charged with Et₃N (1.35 mL, 9.25 mmol) followed by methanesulfonyl chloride (0.75 mL, 9.25 mmol) at 0° C. then stirred at rt for 1 h. Water (200 mL) was added to the reaction mixture and extracted with CH₂Cl₂ (3×200 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, and concentrated to afford crude mesylate of 26 (1.70 g) as brown oil which was directly used for the next step without further purification.

Crude mesylate of 106 (1.70 g) was dissolved in DMF (50 mL) was charged with KSAc (1.28 g, 11.30 mmol) and stirred at rt for 2 h. The reaction mixture was partitioned between water (100 mL) and EtOAc (250 mL). The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×300 mL). The combined organic extracts were concentrated and the residue purified by column chromatography (silica gel, 10% to 20% EtOAc in hexanes) to afford compound 107 (1.20 g, 83% over two steps) as a yellow oil: ¹H NMR (CDCl₃, 400 MHz): δ 7.21 (d, J=7.8 Hz, 1H), 7.10 (br s, 1H), 7.03-6.99 (m, 1H), 4.52 (br s, 1H), 4.10 (s, 2H), 3.16-3.06 (m, 2H), 2.57 (t, J=7.8 Hz, 2H), 2.35 (s, 3H), 2.34 (s, 3H), 1.80-1.71 (m, 2H), 1.44 (s, 9H); ESI-LCMS m/z 412 (M+H)⁴.

Preparation of S,S′-((4-(3-aminopropyl)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (108)

Compound 107 (1.20 g, 2.91 mmol) was dissolved in 4 N HCl in dioxane (12 mL) at room temperature, and the solution was stirred at rt for 2 h. After removal of the solvent, the residue was triturated with EtOAc to afford hydrochloric acid salt 108 (720 mg, 79%) as an off-white solid: ¹H NMR (DMSO-d6, 400 MHz): δ 7.80 (br s, 3H), 7.21 (d, J=7.8 Hz, 1H), 7.13 (br s, 1H), 7.08-7.05 (m, 1H), 4.13 (s, 2H), 4.12 (s, 2H), 2.76 (br s, 2H), 2.58 (t, J=7.6 Hz, 2H), 2.35 (s, 3H), 2.34 (s, 3H), 1.83-1.75 (m, 2H); ESI-LCMS m/z 312 (M+H)⁺.

Preparation of S,S′-((4-(3-(bis((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl) amino) propyl)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (109)

A solution of amine 108 (300 mg, 0.96 mmol) in methanol (30 mL) was charged with D-glucose (1.05 g, 5.78 mmol) and acetic acid (0.35 mL, 5.78 mmol) successively followed by Sodium cyanoborohydride (370 mg, 5.78 mmol) and the resulting reaction mixture was heated 50° C. and stirred at 50° C. for 4 h. After the solvent was removed under reduced pressure, the residue was acidified with 4 N aq.HCl and purified by reverse-phase chromatography using a C18 Gold column to get 109 (55 mg, 9%) as a hygroscopic white solid; (Acetate migrated and acetate cleaved product was observed as major); ¹H NMR (CD₃OD, 400 MHz): δ 7.21-7.16 (m, 2H), 7.12-7.06 (m, 1H), 4.56 (br s, 2H), 4.21-4.02 (m, 5H), 3.84-3.56 (m, 10H), 3.16 (br s, 2H), 2.73-2.57 (m, 2H), 2.33 (s, 3H), 2.32 (s, 3H), 2.09-1.96 (m, 2H); ESI (m/z) 640 [C₂₇H₄₅NO₂S₂+H]⁺.

54. Preparation of (2R,2′R,3R,3′R,4R,4′R,5S,5′S)-6,6′-((3-(3,4-bis (mercaptomethyl) phenyl)propyl)azanediyl)bis(hexane-1,2,3,4,5-pentaol) hydrochloride (110)

A solution of 109 (300 mg, 0.46 mmol) in water (20 mL) and charged with solid LiOH.H₂O (100 mg, 2.34 mmol) and the reaction mixture was stirred at room temperature for 1 h. The above reaction mixture was charged with TCEP.HCl (15 mg, 0.046 mmol) and stirred for another 1 h. The pH of above reaction mixture was adjusted to 2 by aqueous 4 N HCl and solvent was removed. The crude HCl salt was purified by reverse-phase column chromatography and lyophilized to afford 110 (215 mg, 63%) as a hygroscopic off-white solid: ¹H NMR (CD₃OD, 400 MHz): δ 7.24-7.18 (m, 2H), 7.11-7.09 (m, 1H), 4.18-4.08 (m, 2H), 3.87-3.74 (m, 8H), 3.72-3.60 (m, 6H), 3.51-3.35 (m, 6H), 2.78-2.63 (m, 2H), 2.16-2.04 (m, 2H); ESI (m/z) 556 [C₂₃H₄₁NO₁₀S₂+H]⁺.

55. Preparation of S,S′-((3-(2-(bis((2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride (111)

111 was prepared in a similar manner to procedure 23 above using the appropriate starting materials.

All of the references cited above throughout this application are incorporated herein by reference. In the event of a conflict between the foregoing description and a reference, the description provided herein controls. 

The invention claimed is:
 1. A compound represented by formula Ia or Ib:

wherein R¹ and R² are each, independently, hydrogen, lower alkyl, halogen or triflouromethyl; R³ and R⁴ are each, independently, hydrogen, lower alkyl, hydroxyl-lower alkyl, phenyl, (phenyl)-lower alkyl, (halophenyl)-lower alkyl, ((lower-alkyl)phenyl)-lower-alkyl, ((lower-alkoxy)phenyl)-lower-alkyl, (naphthyl)-lower-alkyl, or (pyridyl)-lower-alkyl; each R⁵ is, independently, hydrogen, halogen, trifluoromethyl, lower alkyl, unsubstituted or substituted phenyl, lower alkyl-thio, phenyl-lower alkyl-thio, lower alkyl-sulfonyl, phenyl-lower alkyl-sulfonyl, OH, —(CH₂)_(m)—OR⁸, —O—(CH₂)_(m)—OR⁸, —(CH₂)_(n)—NR⁷R¹⁰, —(CH₂)_(n)—NR⁷R⁷, —O—(CH₂)_(m)—NR⁷R¹⁰, —O—(CH₂)_(m)—NR⁷R⁷, —(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —(CH₂CH₂O)_(m)—R⁸, —O—(CH₂CH₂O)_(m)—R⁸, —(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —O—(CH₂CH₂O)_(m)—CH₂CH₂NR⁷R¹⁰, —(CH₂)_(n)—C(═O)NR⁷R¹⁰, —O—(CH₂)_(m)—C(═O)NR⁷R¹⁰, —(CH₂)_(n)—(Z)_(g)—R⁷, —O—(CH₂)_(m)—(Z)_(g)—R⁷, —(CH₂)_(n)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —O—(CH₂)_(m)—NR¹⁰—CH₂(CHOR⁸)(CHOR⁸)_(n)—CH₂OR⁸, —(CH₂)_(n)—CO₂R⁷, —O—(CH₂)_(m)—CO₂R⁷, —OSO₃H, —O-glucuronide, —O-glucose,

-Link-(CH₂)_(m)-CAP, -Link-(CH₂)_(n)(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂CH₂O)_(m)—CH₂-CAP, -Link-(CH₂CH₂O)_(m)—CH₂CH₂-CAP, -Link-(CH₂)_(m)—(Z)_(g)-CAP, -Link-(CH₂)_(n)(Z)_(g)—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—NR¹³—CH₂(CHOR⁸)(CHOR⁸)_(n)-CAP, -Link-(CH₂)_(n)—(CHOR⁸)_(m)CH₂—NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(n)NR¹³—(CH₂)_(m)(CHOR⁸)_(n)CH₂NR¹³—(Z)_(g)-CAP, -Link-(CH₂)_(m)—(Z)_(g)—(CH₂)_(m)-CAP, -Link-NH—C(═O)—NH—(CH₂)_(m)-CAP, -Link-(CH₂)_(m)—C(═O)NR¹³—(CH₂)_(m)-CAP, -Link-(CH₂)_(n)—(Z)_(g)—(CH₂)_(m)—(Z)_(g)-CAP, or -Link-Z_(g)—(CH₂)_(m)-Het-(CH₂)_(m)-CAP, with the proviso that at least one R⁵ group contains at least one basic nitrogen; each R⁷ is, independently, phenyl, substituted phenyl, lower alkyl phenyl or —CH₂(CHOR⁸)_(m)—CH₂OR⁸; each R⁸ is, independently, hydrogen, lower alkyl, lower alkyl phenyl, —C(═O)—R¹, glucuronide, 2-tetrahydropyranyl, or

each R⁹ is, independently, —CO₂R⁷, —CON(R⁷)₂, —SO₂CH₃, —C(═O)R⁷, —CO₂R¹³, —CON(R¹³)₂, —SO₂CH₂R¹³, or —C(═O)R¹³; each R¹⁰ is, independently, —H, —SO₂CH₃, —CO₂R⁷, —C(═O)NR⁷R⁹, —C(═O)R⁷, or —CH₂—(CHOH)_(n)—CH₂OH; each Z is, independently, —(CHOH)—, —C(═O)—, —(CHNR⁷R¹⁰)—, —(C═NR¹⁰)—, —NR¹⁰—, —(CH₂)_(n)—, —(CHNR¹³R¹³)—, —(C═NR¹³)—, or —NR¹³—; each R¹¹ is, independently, hydrogen, lower alkyl, phenyl lower alkyl or substituted phenyl lower alkyl; each R¹² is, independently, —SO₂CH₃, —CO₂R⁷, —C(═O)NR⁷R⁹, —C(═O)R⁷, —CH₂(CHOH)_(n)—CH₂OH, —CO₂R¹³, —C(═O)NR¹³R¹³, or —C(═O)R¹³; each R¹³ is, independently, hydrogen, lower alkyl, phenyl, substituted phenyl or —CH₂(CHOR⁸)_(m)—CH₂OR⁸, —SO₂CH₃, —CO₂R⁷, —C(═O)NR⁷R⁹, —C(═O)R⁷, —CH₂—(CHOH)_(n)—CH₂OH, —(CH₂)_(m)—NR⁷R¹⁰, —(CH₂)_(m)—NR⁷R⁷, —(CH₂)_(m)—NR¹¹R¹¹, —(CH₂)_(m)—(NR¹¹R¹¹R¹¹)⁺, —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)NR¹¹R¹¹, —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)NR⁷R¹⁰, —(CH₂)_(m)—NR¹⁰R¹⁰, —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)—(NR¹¹R¹¹R¹¹)⁺, or —(CH₂)_(m)—(CHOR⁸)_(m)—(CH₂)_(m)NR⁷R⁷; each R¹⁴ is, independently, —C(═O)—R⁷, —C(═O)-lower alkyl, or an amino acyl of the natural configuration; each g is, independently, an integer from 1 to 6; each m is, independently, an integer from 1 to 7; each n is, independently, an integer from 0 to 7; each -Het- is, independently, —N(R⁷)—, —N(R¹⁰)—, —S—, —SO—, —SO₂—; —O—, —SO₂NH—, —NHSO₂—, —NR⁷CO—, —CONR⁷—, —N(R¹³)—, —SO₂NR¹³—, —NR¹³CO—, or —CONR¹³—; each Link is, independently, —O—, —(CH₂)_(n)—, —O(CH₂)_(m)—, —NR¹³—C(═O)—NR¹³—, —NR¹³—C(═O)—(CH₂)_(m)—, —C(═O)NR¹³—(CH₂)_(m) ⁻, —(CH₂)_(n)—(Z)_(g)—(CH₂)_(n)—, —S—, —SO—, —SO₂—, —SO₂NR⁷—, —SO₂NR¹⁰—, or -Het-; each CAP is, independently

with the proviso that when any —CHO⁸— or —CH₂OR⁸ groups are located 1,2- or 1,3- with respect to each other, the R⁸ groups may, optionally, be taken together to form a cyclic mono- or di-substituted 1,3-dioxane or 1,3-dioxolane; or racemates, enantiomers, diastereomers, tautomers, polymorphs, pseudopolymorphs or pharmaceutically acceptable salts thereof.
 2. A method of liquefying mucus from mucosal surfaces, comprising: administering an effective amount of the compound of claim 1 to a mucosal surface of a subject in need thereof.
 3. A method of treating chronic bronchitis, treating bronchiectasis, treating cystic fibrosis, treating chronic obstructive pulmonary disease, treating asthma, treating sinusitis, treating vaginal dryness, treating dry eye, promoting ocular hydration, promoting corneal hydration, promoting mucus clearance in mucosal surfaces, treating Sjogren's disease, treating distal intestinal obstruction syndrome, treating dry skin, treating esophagitis, treating dry mouth, treating nasal dehydration, treating ventilator-induced pneumonia, treating asthma, treating primary ciliary dyskinesia, treating otitis media, inducing sputum for diagnostic purposes, treating cystinosis, treating emphysema, treating pneumonia, treating constipation, treating chronic diverticulitis, and/or treating rhinosinusitis, comprising: administering an effective amount of the compound of claim 1 to a subject in need thereof.
 4. A method of treating an eye disease characterized by the presence of ocular discharge comprising administering to a subject in need thereof an effective amount of the compound of claim 1, wherein the eye disease is one or more conditions selected from the group consisting of blepharitis, allergies, conjunctivitis, corneal ulcer, trachoma, congenital herpes simplex, corneal abrasions, ectropion, eyelid disorders, gonococcal conjunctivitis, herpetic keratitis, ophthalmitis, Sjogren's Syndrome and Stevens-Johnson Syndrome.
 5. A method of treating a disease ameliorated by increased mucociliary clearance and mucosal hydration comprising administering to a subject in need of increased mucociliary clearance and mucosal hydration an effective amount of an osmolyte and the compound of claim 1, wherein the disease is one or more conditions selected from the group consisting of chronic bronchitis, bronchiectasis, cystic fibrosis, asthma, sinusitis, vaginal dryness, dry eye, Sjogren's disease, distal intestinal obstruction syndrome, dry skin, esophagitis, dry mouth (xerostomia), nasal dehydration, asthma, primary ciliary dyskinesia, otitis media, chronic obstructive pulmonary disease, emphysema, pneumonia, diverticulitis, rhinosinusitis and airborne infections.
 6. The method of claim 5, wherein the compound is administered preceding administration of the osmolyte.
 7. The method of claim 5, wherein the compound is administered concurrent with administration of the osmolyte.
 8. The method of claim 5, wherein the compound is administered following administration of the osmolyte.
 9. The method of claim 5, wherein the osmolyte is hypertonic saline or mannitol.
 10. The method of claim 5, wherein the osmolyte is sodium chloride which is delivered as a micronized particle of respirable size.
 11. The method of claim 5, wherein the effective amount of an osmolyte and the compound is administered by aerosolization using a device capable of delivering the formulation to the nasal passages or pulmonary airway wherein the aerosol is a respirable size.
 12. A composition, comprising: (a) the compound of claim 1 and (b) an osmotically active compound.
 13. A method of inducing sputum, comprising administering to a subject in need of increased mucociliary clearance and mucosal hydration an effective amount of an osmolyte and the compound of claim
 1. 14. A method of therapeutic treatment against diseases or conditions caused by pathogens, comprising administering to a subject in need of increased mucociliary clearance and mucosal hydration an effective amount of the compound of claim
 1. 15. The method of claim 14, wherein the pathogen is anthrax or plague.
 16. A method for mitigating, and/or treating deterministic health effects to the respiratory tract and/or other bodily organs caused by respirable aerosols containing radionuclides in a human in need thereof, said method comprising administering to said human an effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof.
 17. A pharmaceutical composition, comprising the compound of claim 1, and a pharmaceutically acceptable carrier.
 18. A method for improving mucus penetration of therapeutic agents comprising administering an effective amount of the compound of claim 1 and a second therapeutic agent to a subject in need thereof.
 19. The method of claim 18, wherein the second therapeutic agents is an osmolyte, a sodium channel blocker, a secretogogue, a bronchodilator, an anti-infective, an anti-inflammatory, or a gene carrier.
 20. A method for decreasing mucosal inflammation comprising administering an effective amount of the compound of claim 1 to a subject in need thereof.
 21. A method for decreasing mucosal oxygen free radicals comprising administering an effective amount of the compound of claim 1 to a subject in need thereof.
 22. The compound of claim 1, which is represented by the formula:


23. The compound of claim 1, which is an acid addition salt of an inorganic acid or an organic acid selected from the group consisting of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, furmaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalensulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, malonic acid, sulfosalicylic acid, glycolic acid, 2-hydroxy-3-naphthoate, pamoate, salicylic acid, stearic acid, phthalic acid, mandelic acid and lactic acid.
 24. A composition containing a pharmaceutically acceptable carrier, hypertonic saline and a compound represented by the formula:

or a pharmaceutically acceptable salt thereof. 